| 疾病名称 |
别名 |
|
| Amyotrophic Lateral Sclerosis 1 |
|
Amyotrophic Lateral Sclerosis
|
ALS
|
|
Lou Gehrig Disease
|
Amyotrophic Lateral Sclerosis Type 1
|
|
Charcot Disease
|
ALS1
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To
|
Fals
|
|
Lou Gehrig'S Disease
|
Mnd
|
|
Motor Neuron Disease
|
Familial Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis 1, Familial
|
Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
|
Motor Neuron Disease, Bulbar
|
Motor Neurone Disease
|
|
Amyotrophic Lateral Sclerosis With Dementia
|
Dementia With Amyotrophic Lateral Sclerosis
|
|
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
|
Sclerosis, Lateral, Amyotrophic
|
|
Sclerosis, Lateral, Amyotrophic, Type 1
|
Amyotrophic Sclerosis
|
|
Als - [Amyotrophic Lateral Sclerosis]
|
Wasting Palsy
|
|
Amyotrophic Paralysis
|
Amyotrophy Lateral Sclerosis
|
|
Wasting Paralysis
|
Spinal Progressive Amyotrophy
|
|
Progressive Atrophic Paralysis
|
|
|
| Spastic Tetraplegia And Axial Hypotonia, Progressive |
|
STAHP
|
Sod1 Deficiency, Autosomal Recessive
|
|
|
| Motor Neuron Disease |
|
Anterior Horn Cell Disease
|
Motor Neuron Diseases
|
|
Mnd - [Motor Neurone Disease]
|
Lou Gehrig Disease
|
|
Creeping Palsy
|
Creeping Paralysis
|
|
Bulbar Motor Neuron Disease
|
Bulbar Syndrome
|
|
Anterior Horn Cell Disorder
|
Hereditary Motor Neuron Disease
|
|
|
| Lateral Sclerosis |
|
Primary Lateral Sclerosis
|
Adult-Onset Primary Lateral Sclerosis
|
|
Adult-Onset Pls
|
Motor Neuron Disease
|
|
Pls
|
Pls - [Primary Lateral Sclerosis]
|
|
Lateral Spinal Sclerosis
|
Lateral Complete Paralysis
|
|
Lateral Incomplete Paralysis
|
Lateral Paralysis
|
|
|
| Eales Disease |
|
Idiopathic Obliterative Vasculopathy
|
Idiopathic Recurrent Vitreal Hemorrhage
|
|
Idiopathic Retinal Perivasculitis
|
Idiopathic Retinal Vasculitis
|
|
|
| Senile Cataract |
|
|
| Mild Pre-Eclampsia |
|
|
| Pneumoconiosis |
|
Pneumoconioses
|
Silicosis Nos
|
|
Complicated Silicosis
|
Fibrosis Of Lung With Silicosis
|
|
Nodular Silicosis
|
Pneumoconiosis Due To Silica
|
|
Silicotic Fibrosis Of Lung
|
Simple Silicosis
|
|
Silicatosis
|
Silicotic Lung Fibrosis
|
|
Pneumoconiosis Due To Talc
|
Pulmonary Talcosis
|
|
Talc Lung Disease
|
Talc Pneumoconiosis
|
|
Talc Workers' Pneumoconiosis
|
Talcosis
|
|
Fibrosis Of Lung Due To Talc
|
Asbestos Pneumoconiosis
|
|
Amianthosis
|
Asbestosis
|
|
Lung Fibrosis With Asbestosis
|
Pulmonary Asbestosis
|
|
|
| Bronchopulmonary Dysplasia |
|
|
| Acne |
|
Acne Vulgaris
|
Acne Varioliformis
|
|
Frontalis Acne
|
|
|
| Postcholecystectomy Syndrome |
|
Post Cholecystectomy Syndrome
|
|
|
| Spinal And Bulbar Muscular Atrophy, X-Linked 1 |
|
Kennedy Disease
|
Sbma
|
|
Spinal And Bulbar Muscular Atrophy
|
Kennedy'S Disease
|
|
X-Linked Spinal And Bulbar Muscular Atrophy
|
SMAX1
|
|
Kd
|
Kennedy Spinal And Bulbar Muscular Atrophy
|
|
Spinobulbar Muscular Atrophy
|
Bulbospinal Muscular Atrophy, X-Linked
|
|
Bulbospinal Neuronopathy, X-Linked Recessive
|
Xbsn
|
|
Spinal And Bulbar Muscular Atrophy Of Kennedy
|
Bulbospinal Muscular Atrophy
|
|
X-Linked Bulbospinal Amyotrophy
|
Bulbo-Spinal Atrophy, X-Linked
|
|
Spinal Bulbar Muscular Atrophy
|
X-Linked Bulbo-Spinal Atrophy
|
|
X-Linked Spinal Bulbar Muscular Atrophy
|
X-Linked Bsma
|
|
X-Linked Bulbospinal Muscular Atrophy
|
Spinal And Bulbar Muscular Atrophy X-Linked 1
|
|
Bulbospinal Muscular Atrophy X-Linked
|
Bulbospinal Neuronopathy X-Linked Recessive
|
|
Kennedy Disease)
|
Kennedy Syndrome
|
|
Atrophy, Muscular, Spinal And Bulbar, Kennedy Type
|
Atrophy, Muscular, Spinobulbar
|
|
Bulbospinal Neuronopathy
|
|
|
| Wilson Disease |
|
Hepatolenticular Degeneration
|
WD
|
|
Wilson'S Disease
|
WND
|
|
Westphal-Strumpell Syndrome
|
Copper Storage Disease
|
|
Cerebral Pseudosclerosis
|
Westphal Pseudosclerosis
|
|
Hepatolenticular Degeneration Syndrome
|
Copper Retention
|
|
Hepatocerebral Degeneration
|
Kinnier-Wilson Disease
|
|
Neurohepatic Degeneration
|
Progressive Hepatolenticular Degeneration
|
|
Lenticular Degenerative Disease
|
Wilson'S Syndrome
|
|
Lenticular Syndrome
|
|
|
| Ischemia |
|
|
| Tonsillitis |
|
Chronic Tonsillitis
|
Throat Infection - Tonsillitis
|
|
|
| Brain Edema |
|
Cerebral Edema
|
Intracranial Swelling
|
|
Wet Brain
|
|
|
| Myocardial Stunning |
|
|
| Amyotrophic Lateral Sclerosis 19 |
|
Amyotrophic Lateral Sclerosis Type 19
|
ALS19
|
|
Sclerosis, Lateral, Amyotrophic, Type 19
|
|
|
| Septooptic Dysplasia |
|
Septo-Optic Dysplasia
|
De Morsier Syndrome
|
|
Growth Hormone Deficiency With Pituitary Anomalies
|
SOD
|
|
Pituitary Hormone Deficiency, Combined, 5
|
Septo-Optic Dysplasia Spectrum
|
|
Septo-Optic Dysplasia With Growth Hormone Deficiency
|
Pituitary Hormone Deficiency, Combined 5
|
|
Hypopituitarism And Septooptic 'Dysplasia'
|
GHDPA
|
|
CPHD5
|
Dysplasia, Septo-Optic
|
|
Kallmann Syndrome
|
|
|
| Spinal Cord Neuroblastoma |
|
Neuroblastoma Of The Spinal Cord
|
|
|
| Spinal Cord Primitive Neuroectodermal Neoplasm |
|
Spinal Cord Pnet
|
Spinal Cord Primitive Neuroectodermal Tumor
|
|
|
| Friedreich Ataxia |
|
Friedreich Ataxia 1
|
FRDA
|
|
Friedreich Ataxia With Retained Reflexes
|
Frda1
|
|
Fa
|
Friedreich'S Ataxia
|
|
Hereditary Spinal Ataxia
|
Fa1
|
|
Friedreich'S Tabes
|
Hereditary Spinal Sclerosis
|
|
Spinocerebellar Ataxia, Friedreich
|
Friedreich Spinocerebellar Ataxia
|
|
Friedrich'S Ataxia
|
|
|
| Methemoglobinemia |
|
|
| Down Syndrome |
|
Trisomy 21
|
Complete Trisomy 21 Syndrome
|
|
Down'S Syndrome
|
Trisomy 21 Syndrome
|
|
Down'S Syndrome - Trisomy 21
|
Downs Syndrome
|
|
G Trisomy
|
47,Xx,+21
|
|
47,Xy,+21
|
Trisomy G
|
|
Down Syndrome, Susceptibility To
|
Chromosome 21 Trisomy
|
|
Trisomy 21 Nos
|
Abnormal Autosomes 21
|
|
|
| Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia |
|
Amyotrophic Lateral Sclerosis Type 10
|
ALS10
|
|
Amyotrophic Lateral Sclerosis 10, With Or Without Ftd
|
Frontotemporal Lobar Degeneration, Tardbp-Related
|
|
Amyotrophic Lateral Sclerosis 10
|
Amyotrophic Lateral Sclerosis 10, With Or Without Frontotemporal Dementia
|
|
Tardbp-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions
|
Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia And With Tdp43 Inclusions
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 10
|
|
|
| Spinocerebellar Ataxia 2 |
|
Spinocerebellar Ataxia Type 2
|
SCA2
|
|
Amyotrophic Lateral Sclerosis 13
|
Spinocerebellar Degeneration With Slow Eye Movements
|
|
SDSEM
|
Spinocerebellar Atrophy Ii
|
|
Olivopontocerebellar Atrophy Ii
|
Opca2
|
|
Cerebellar Degeneration With Slow Eye Movements
|
Wadia-Swami Syndrome
|
|
Amyotrophic Lateral Sclerosis Type 13
|
ALS13
|
|
Olivopontocerebellar Atrophy Holguin Type
|
Spinocerebellar Ataxia Cuban Type
|
|
Olivopontocerebellar Atrophy, Holguin Type
|
Spinocerebellar Ataxia, Cuban Type
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To, 13
|
Olivopontocerebellar Atrophy 2
|
|
Sca 2
|
Spinocerebellar Ataxia With Slow Eye Movements
|
|
Spinocerebellar Atrophy 2
|
Wadia Swami Syndrome
|
|
Opca Ii
|
Spinocerebellar Ataxia-2
|
|
Ataxia, Spinocerebellar, Type 2
|
|
|
| Hyperekplexia |
|
Hereditary Hyperekplexia
|
Kok Disease
|
|
Congenital Stiff Man Syndrome
|
Familial Startle Disease
|
|
Sthe
|
Stiff-Baby Syndrome
|
|
Hereditary Hyperexplexia
|
Startle Disease
|
|
Exaggerated Startle Reaction
|
Hyperexplexia Hereditary
|
|
Startle Disease, Familial
|
Startle Reaction, Exaggerated
|
|
Stiff-Man Syndrome, Congenital
|
Stiff-Person Syndrome, Congenital
|
|
Congenital Stiff-Man Syndrome
|
Congenital Stiff-Person Syndrome
|
|
Familial Hyperekplexia
|
Startle Syndrome
|
|
Stiff Baby Syndrome
|
Hyperekplexia, Hereditary
|
|
Stiff-Person Syndrome
|
|
|
| Frontotemporal Dementia |
|
Pallidopontonigral Degeneration
|
Frontotemporal Lobar Degeneration
|
|
Semantic Dementia
|
FTD
|
|
Frontotemporal Lobe Dementia
|
Multiple System Tauopathy With Presenile Dementia
|
|
Dementia, Frontotemporal
|
Frontotemporal Dementia With Parkinsonism
|
|
Mstd
|
Frontotemporal Lobar Degeneration With Tau Inclusions
|
|
Ftld With Tau Inclusions
|
Dementia, Frontotemporal, With Parkinsonism
|
|
Fldem
|
Ftdp17
|
|
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex
|
Ddpac
|
|
Wilhelmsen-Lynch Disease
|
Wld
|
|
Ppnd
|
Dementia, Frontotemporal, With Or Without Parkinsonism
|
|
Semantic Primary Progressive Aphasia
|
Semantic Variant Ppa
|
|
Wilhemsen-Lynch Disease
|
Frontotemporal Dementia-Amyotrophic Lateral Sclerosis
|
|
Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17
|
Ftd-Als
|
|
Ftld
|
Pick Complex
|
|
Pick Disease Of The Brain
|
Frontotemporal Dementia With Parkinsonism-17
|
|
Grn-Related Frontotemporal Dementia
|
Frontotemporal Dementia With Motor Neuron Disease
|
|
Dementia In Fronto-Temporal Lobar Degeneration
|
Ftd - [Frontotemporal Dementia]
|
|
Temple Dementia
|
Frontal Lobe Dementia
|
|
|
| Amyotrophic Lateral Sclerosis Type 6 |
|
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
|
Als6
|
|
Amyotrophic Lateral Sclerosis 6, With Or Without Frontotemporal Dementia
|
Autosomal Recessive Amyotrophic Lateral Sclerosis 6
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 6
|
Amyotrophic Lateral Sclerosis 6
|
|
|
| Amyotrophic Lateral Sclerosis 4, Juvenile |
|
Amyotrophic Lateral Sclerosis Type 4
|
ALS4
|
|
Amyotrophic Lateral Sclerosis 4
|
Dhmn With Upper Motor Neuron Signs
|
|
Distal Hereditary Motor Neuropathy With Upper Motor Neuron Signs
|
Neuronopathy, Distal Hereditary Motor, With Pyramidal Features
|
|
Als 4
|
Distal Hereditary Motor Neuropathy With Pyramidal Features
|
|
Amyotrophic Lateral Sclerosis Juvenile 4
|
Neuronopathy Distal Hereditary Motor With Pyramidal Features
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 4
|
|
|
| Uremia |
|
|
| Hyperhomocysteinemia |
|
|
| Retinal Vasculitis |
|
|
| Amyotrophic Lateral Sclerosis 2, Juvenile |
|
ALS2
|
Als, Juvenile
|
|
Alsj
|
Amyotrophic Lateral Sclerosis Type 2
|
|
Amyotrophic Lateral Sclerosis 2
|
Amyotrophic Lateral Sclerosis Type 2, Juvenile
|
|
Amyotrophic Lateral Sclerosis Juvenile
|
Amyotrophic Lateral Sclerosis Juvenile 2
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 2
|
|
|
| Hyperglycemia |
|
|
| Amyotrophic Lateral Sclerosis 20 |
|
Amyotrophic Lateral Sclerosis Type 20
|
ALS20
|
|
Sclerosis, Lateral, Amyotrophic, Type 20
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2e |
|
Charcot-Marie-Tooth Disease Type 2
|
CMT2E
|
|
CMT2S
|
CMT2Y
|
|
Charcot-Marie-Tooth Disease Type 2e
|
Charcot-Marie-Tooth Disease Type 2y
|
|
Charcot-Marie-Tooth Disease Axonal Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Type 2s
|
|
Charcot-Marie-Tooth Disease, Type 2e
|
Hereditary Motor And Sensory Neuropathy Type 2
|
|
Charcot-Marie-Tooth Neuropathy, Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s
|
|
Charcot-Marie-Tooth Disease, Axonal, Type 2y
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y
|
|
Charcot-Marie-Tooth Neuropathy, Type 2y
|
Charcot-Marie-Tooth Disease, Type 2y
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e
|
Charcot-Marie-Tooth Neuropathy Type 2e
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation
|
Cmt2 Due To Vcp Mutation
|
|
Charcot-Marie-Tooth Disease Type 2s
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2
|
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Disease
|
Cmt2
|
|
Charcot-Marie-Tooth Neuropathy, Type 2e
|
Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type
|
|
Hereditary Motor And Sensory Neuropathy Okinawa Type
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y
|
|
Charcot-Marie-Tooth Neuropathy Type 2y
|
Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s
|
|
Charcot-Marie-Tooth Neuropathy Type 2s
|
Charcot-Marie-Tooth Type 2
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y
|
Charcot-Marie-Tooth Disease 2e
|
|
Charcot-Marie-Tooth Disease Axonal Type 2e
|
Charcot-Marie-Tooth Disease Neuronal Type 2e
|
|
Charcot-Marie-Tooth Disease 2s
|
Charcot-Marie-Tooth Neuropathy Axonal Type 2s
|
|
Charcot-Marie-Tooth Disease 2y
|
Charcot-Marie-Tooth Disease, Type 2
|
|
Hereditary Motor And Sensory-Neuropathy Type Ii
|
|
|
| Progressive Muscular Atrophy |
|
Progressive Spinal Muscular Atrophy
|
Pure Progressive Muscular Atrophy
|
|
Pma
|
Hereditary Spinal Muscle Atrophy
|
|
Pma - [Progressive Muscular Atrophy]
|
Progressive Muscle Atrophy
|
|
Progressive Spinal Muscle Atrophy
|
Duchenne-Aran Atrophy
|
|
Duchenne-Aran Muscle Atrophy
|
Hereditary Sma - [Spinal Muscle Atrophy]
|
|
|
| Amyotrophic Lateral Sclerosis 8 |
|
Amyotrophic Lateral Sclerosis Type 8
|
ALS8
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 8
|
|
|
| Progressive Bulbar Palsy |
|
Bulbar Palsy, Progressive
|
Progressive Bulbar Atrophy
|
|
Bulbar Palsy
|
Pbp - [Progressive Bulbar Palsy]
|
|
Progressive Bulbar Paralysis
|
Bulbar Paralysis
|
|
Chronic Bulbar Palsy
|
Chronic Bulbar Paralysis
|
|
Supranuclear Bulbar Paralysis
|
|
|
| Pancreatitis |
|
|
| Menkes Disease |
|
Copper Transport Disease
|
Menkes Syndrome
|
|
MNK
|
Kinky Hair Disease
|
|
Steely Hair Disease
|
Menkes Kinky-Hair Syndrome
|
|
Mk
|
Steely Hair Syndrome
|
|
Menkea Syndrome
|
Md
|
|
Menkes Kinky Hair Syndrome
|
Hypocupremia, Congenital
|
|
Kinky Hair Syndrome
|
X-Linked Copper Deficiency
|
|
Menkes Kinky Hair Disease
|
|
|
| Keratoconus |
|
Kc
|
Conical Cornea
|
|
Noninflammatory Corneal Thining
|
Bulging Cornea
|
|
Cornea Conical
|
Acquired Conus Of Cornea
|
|
|
| Varicocele |
|
Scrotal Varices
|
Varicoceles
|
|
Varicocele Of Scrotum
|
Scrotal Varicocele
|
|
|
| Erysipelas |
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 4 |
|
FTDALS4
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-4
|
|
Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 4
|
|
|
| Pre-Eclampsia |
|
Preeclampsia
|
Gestational Hypertension
|
|
Hypertension Induced By Pregnancy
|
Pre-Eclamptic Toxaemia
|
|
Pregnancy Associated Hypertension
|
Proteinuric Hypertension Of Pregnancy
|
|
Hypertension, Pregnancy-Induced, Susceptibility To
|
Preeclampsia/Eclampsia
|
|
Pregnancy Toxemia
|
Toxaemia Of Pregnancy
|
|
Gestational Proteinuric Hypertension
|
Pregnancy-Induced Hypertension
|
|
Toxemia Of Pregnancy
|
Preeclampsia, Susceptibility To
|
|
Transient Hypertension Of Pregnancy
|
Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria
|
|
Gestational Hypertension Nos
|
Mild Proteinuric Hypertension Of Pregnancy
|
|
Pih - [Pregnancy-Induced Hypertension]
|
Pregnancy-Induced Hypertension Nos
|
|
Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria
|
Pe - [Pre-Eclampsia]
|
|
Pre-Eclampsia Nos
|
Pre-Eclamptic Nos
|
|
Pregnancy Pre-Eclampsia
|
Puerperal Pre-Eclampsia
|
|
Pre-Eclampsia Toxaemia
|
Toxaemia In Pregnancy
|
|
Pet - [Pre-Eclamptic Toxaemia]
|
Maternal Toxaemia
|
|
|
| Porphyria, Acute Intermittent |
|
Acute Intermittent Porphyria
|
Porphobilinogen Deaminase Deficiency
|
|
Pbgd Deficiency
|
AIP
|
|
Porphyria, Swedish Type
|
Uroporphyrinogen Synthase Deficiency
|
|
Ups Deficiency
|
Porphyria, Acute Intermittent, Nonerythroid Variant
|
|
Hydroxymethylbilane Synthase Deficiency
|
Aip - Acute Intermittent Porphyria
|
|
Porphyria Intermittent Acute
|
Pyrroloporphyria
|
|
Hmbs Deficiency
|
Porphyria Acute Intermittent
|
|
|
| Acute Pancreatitis |
|
Pancreatitis
|
Pancreatitis, Acute Necrotizing
|
|
Pancreatitis Nos
|
Acute Pancreas Inflammation
|
|
|
| Lung Disease |
|
Lung Diseases
|
Disorder Of Lung
|
|
Abnormality Of The Lung
|
|
|
| Exfoliation Syndrome |
|
Pseudoexfoliation Glaucoma
|
Pseudoexfoliation Syndrome
|
|
Exfoliation Syndrome, Susceptibility To
|
XFS
|
|
Exfoliation Glaucoma
|
Xfg
|
|
Pseudoexfoliation Of The Lens
|
Pexg
|
|
Pexs
|
Exfoliative Syndrome
|
|
Glaucoma Capsulare
|
Pex
|
|
Pseudo-Exfoliation Syndrome
|
|
|
| Atrophic Gastritis |
|
Gastritis, Atrophic
|
Gastric Atrophy
|
|
Gastritis Atrophic
|
|
|
| Amyotrophic Lateral Sclerosis 11 |
|
Amyotrophic Lateral Sclerosis Type 11
|
ALS11
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 11
|
|
|
| Parkinson Disease, Late-Onset |
|
Parkinson Disease
|
Parkinson'S Disease
|
|
PD
|
PARK
|
|
Parkinson Disease, Susceptibility To
|
Late Onset Parkinson'S Disease
|
|
Late Onset Parkinson Disease
|
Paralysis Agitans
|
|
Primary Parkinsonism
|
Idiopathic Parkinson Disease
|
|
Parkinson'S
|
Parkinson Disease, Late-Onset, Susceptibility To
|
|
Parkinson Disease, Age Of Onset, Modifier
|
Lewy Body Parkinson Disease
|
|
Idiopathic Parkinson'S Disease
|
Pd - [Parkinson Disease]
|
|
Parkinson Disease Nos
|
Parkinson, Nos
|
|
Primary Parkinson Disease
|
|
|
| Locked-In Syndrome |
|
Locked In Syndrome
|
Cerebromedullospinal Disconnection
|
|
Locked-In State
|
Quadriplegia
|
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1 |
|
FTDALS1
|
Frontotemporal Dementia And/Or Motor Neuron Disease
|
|
Ftdmnd
|
Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia
|
|
Alsftd
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis
|
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1
|
Frontotemporal Dementia With Motor Neuron Disease
|
|
Ftdals
|
Ftd-Als
|
|
Ftd-Mnd
|
Frontotemporal Dementia With Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1
|
Amyotrophic Lateral Sclerosis/Frontotemporal Dementia
|
|
Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis
|
Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1
|
|
Frontotemporal Lobar Degeneration
|
Grn-Related Frontotemporal Dementia
|
|
|
| Bacterial Meningitis |
|
Meningitis, Bacterial
|
Meningitis Bacterial
|
|
Bm - [Bacterial Meningitis]
|
Leptomeningitis Bacterial
|
|
Pachymeningitis Bacterial
|
Arachnoiditis Bacterial
|
|
|
| Amyotrophic Lateral Sclerosis 18 |
|
Amyotrophic Lateral Sclerosis Type 18
|
ALS18
|
|
Sclerosis, Lateral, Amyotrophic, Type 18
|
|
|
| Male Infertility |
|
Infertility, Male
|
Infertility Male
|
|
Male Sterility
|
Absolute Infertility
|
|
|
| Creutzfeldt-Jakob Disease |
|
Variant Creutzfeldt-Jakob Disease
|
CJD
|
|
Bovine Spongiform Encephalopathy
|
Vcjd
|
|
Inherited Creutzfeldt-Jakob Disease
|
Creutzfeldt-Jakob Disease, Familial
|
|
Creutzfeldt Jakob Disease
|
Creutzfeldt-Jacob Disease
|
|
Creutzfeldt Jacob Disease
|
Sporadic Creutzfeldt-Jakob Disease
|
|
Encephalopathy, Bovine Spongiform
|
Creutzfeldt-Jakob Disease, Variant, Resistance To
|
|
Creutzfeldt-Jakob Disease, Variant
|
Creutzfeldt Jacob Syndrome
|
|
Jakob-Creutzfeldt Disease
|
Subacute Spongiform Encephalopathy
|
|
Transmissible Virus Dementia
|
New Variant Of Cjd
|
|
Nv-Cjd
|
Variant Cjd
|
|
Variant Creutzfeldt-Jacob Disease
|
Sporadic Cjd
|
|
Inherited Cjd
|
Acquired Creutzfeldt-Jakob Disease
|
|
Variant Mcj
|
Encephalopathy Bovine Spongiform
|
|
Familial Creutzfeldt-Jakob Disease
|
Creutzfeldt-Jakob Syndrome
|
|
New Variant Creutzfeldt-Jakob Disease
|
Creutzfeldt-Jakob Disease, Sporadic
|
|
Acquired Cjd
|
Scjd - [Sporadic Creutzfeldt-Jakob Disease]
|
|
Idiopathic Creutzfeldt-Jakob Disease
|
Creutzfeld-Jakob Disease Nos
|
|
Vcjd - [Variant Creutzfeldt-Jakob Disease]
|
|
|
| Amyotrophic Lateral Sclerosis 16, Juvenile |
|
Amyotrophic Lateral Sclerosis Type 16
|
ALS16
|
|
Amyotrophic Lateral Sclerosis 16
|
Sclerosis, Lateral, Amyotrophic, Type 16, Juvenile
|
|
|
| Amyotrophic Lateral Sclerosis Type 12 |
|
Amyotrophic Lateral Sclerosis 12
|
Als12
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 12
|
|
|
| Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 |
|
Guam Disease
|
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex Of Guam
|
|
Als-Pdc
|
Lytico-Bodig Disease
|
|
Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex
|
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1, Susceptibility To
|
|
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex, Susceptibility To
|
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex
|
|
Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Of Guam Syndrome
|
Parkinsonism-Dementia-Als Complex
|
|
Pdals
|
Amyotrophic Lateral Sclerosis, Parkinsonism/Dementia Complex Of Guam
|
|
Parkinson-Dementia Complex Of Guam
|
G-Pdc
|
|
Guam Parkinsonism-Dementia Complex
|
ALS-PDC1
|
|
Als/Pdc Of Guam
|
Amyotrophic Lateral Sclerosis
|
|
Sclerosis, Lateral, Amyotrophic/Parkinsonism/Dementia Complex 1
|
Amyotrophic Lateral Sclerosis, Guam Form
|
|
Parkinsonian Disorders
|
|
|
| Maple Syrup Urine Disease |
|
MSUD
|
Bckd Deficiency
|
|
Branched-Chain Ketoaciduria
|
Branched-Chain Alpha-Keto Acid Dehydrogenase Deficiency
|
|
Keto Acid Decarboxylase Deficiency
|
Maple Syrup Urine Disease, Type Ii
|
|
Branched Chain Ketoaciduria
|
Classic Maple Syrup Urine Disease
|
|
Intermittent Maple Syrup Urine Disease
|
Maple Syrup Urine Disease, Type Ia
|
|
Ketoacidaemia
|
Bckdh Deficiency
|
|
Branched-Chain 2-Ketoacid Dehydrogenase Deficiency
|
Thiamine-Responsive Maple Syrup Urine Disease
|
|
Intermediate Maple Syrup Urine Disease
|
Maple Syrup Urine Disease Type 1a
|
|
Maple Syrup Urine Disease Type 1b
|
Maple Syrup Urine Disease Type 2
|
|
Maple Syrup Urine Disease, Type Ib
|
Dihydrolipoamide Dehydrogenase Deficiency
|
|
Branched-Chain Ketoacid Dehydrogenase Deficiency
|
Maple Syrup Disease
|
|
Ketoacidemia
|
Classic Bckd Deficiency
|
|
Classic Msud
|
Classic Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency
|
|
Classic Branched-Chain Ketoaciduria
|
Thiamine-Responsive Bckd Deficiency
|
|
Thiamine-Responsive Msud
|
Thiamine-Responsive Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency
|
|
Intermittent Bckd Deficiency
|
Intermittent Msud
|
|
Intermittent Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency
|
Maple Syrup Urine Disease 1a
|
|
MSUD1A
|
Maple Syrup Urine Disease Type Ia
|
|
Msud Type Ia
|
Maple Syrup Urine Disease 1b
|
|
MSUD1B
|
Maple Syrup Urine Disease Type Ib
|
|
Msud Type Ib
|
Maple Syrup Urine Disease 2
|
|
MSUD2
|
Maple Syrup Urine Disease Type Ii
|
|
Msud Type Ii
|
Nadh Cytochrome B5 Reductase Deficiency
|
|
Lactic Acidosis, Congenital Infantile, Due To Lad Deficiency
|
Ketonemia
|
|
Maple Syrup Urine Disease, Type 1b
|
Ketoacid Decarboxylase Deficiency
|
|
Oxoacid Decarboxylase Deficiency
|
Branched Chain Ketoacid Dehydrogenase Deficiency
|
|
Msud - [Maple-Syrup-Urine Disease]
|
Ketoaminoacidaemia
|
|
Bckd - [Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency]
|
Maple-Syrup-Urine Disorder
|
|
Maple-Syrup-Urine Syndrome
|
|
|
| Tetanus |
|
Lockjaw
|
Clostridial Tetanus
|
|
Infection Due To Clostridium Tetani
|
Lock-Jaw
|
|
|
| Cataract |
|
Cataracts
|
Cat - [Cataract]
|
|
Cataract Form
|
Lens Opacity
|
|
Lens Opacities
|
|
|
| Diabetes Mellitus |
|
|
| Spinal Muscular Atrophy |
|
Sma
|
5q Sma
|
|
Proximal Sma
|
Sma-Associated Sma
|
|
Spinal Amyotrophies
|
Spinal Amyotrophy
|
|
Spinal Muscle Degeneration
|
Spinal Muscle Wasting
|
|
Muscular Atrophy Spinal
|
Atrophy, Muscular, Spinal
|
|
Hereditary Motor Neuronopathy
|
Progressive Muscular Atrophy
|
|
Sma - [Spinal Muscular Atrophy]
|
|
|
| Chronic Granulomatous Disease |
|
Cgd
|
Granulomatous Disease, Chronic
|
|
Autosomal Recessive Chronic Granulomatous Disease
|
X-Linked Chronic Granulomatous Disease
|
|
Bridges-Good Syndrome
|
Congenital Dysphagocytosis
|
|
Quie Syndrome
|
Chronic Septic Granulomatosis
|
|
Chronic Granulomatous Disorder
|
Granulomatous Disease Chronic
|
|
Granulomatous Disease, Chronic, X-Linked
|
|
|
| Type 2 Diabetes Mellitus |
|
Insulin Resistance
|
NIDDM
|
|
Type 2 Diabetes
|
Diabetes Mellitus, Non-Insulin-Dependent
|
|
T2D
|
Noninsulin-Dependent Diabetes Mellitus
|
|
Diabetes Mellitus, Type Ii
|
Maturity-Onset Diabetes
|
|
Insulin Resistance, Severe, Digenic
|
Diabetes Mellitus, Type 2
|
|
Diabetes Mellitus, Noninsulin-Dependent
|
Diabetes Mellitus, Noninsulin-Dependent, Association With
|
|
Diabetes Mellitus, Noninsulin-Dependent, Late Onset
|
Hypertension, Insulin Resistance-Related, Susceptibility To
|
|
Insulin Resistance, Susceptibility To
|
Non-Insulin-Dependent Diabetes Mellitus
|
|
Type Ii Diabetes Mellitus
|
Adult-Onset Diabetes Mellitus
|
|
Maturity-Onset Diabetes Mellitus
|
Diabetes Mellitus Type 2
|
|
Type Ii Diabetes
|
Type 2 Diabetes Mellitus, Susceptibility To
|
|
Diabetes, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
|
|
Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 2, Susceptibility To
|
|
Diabetes Mellitus, Noninsulin-Dependent, 2
|
Diabetes Mellitus, Type Ii, Susceptibility To
|
|
Hypertension, Insulin Resistance-Related
|
Adult-Onset Diabetes
|
|
Aodm
|
Diabetes Mellitus, Adult-Onset
|
|
Diabetes Mellitus Type Ii
|
Diabetes Mellitus Type 2, Susceptibility To
|
|
Diabetes, Type Ii, Susceptibility To
|
Diabetes Type 2
|
|
Diabetes Mellitus
|
Adult Onset Diabetes
|
|
Maturity Onset Diabetes
|
Nonketotic Diabetes
|
|
Non-Insulin Dependent Diabetes Mellitus
|
T2dm - [Type 2 Diabetes Mellitus]
|
|
Niddm - [Non Insulin Dependent Diabetes Mellitus]
|
Dm2
|
|
Dm Type Ii
|
Diabetic Type 2
|
|
Insulin Requiring Type 2 Diabetes
|
Noninsulin Dependent Diabetes
|
|
Non-Insulin-Dependent Diabetes Mellitus Without Complications
|
Diabetes Due To Insulin Secretory Defect
|
|
Diabetes Mellitus Due To Insulin Secretory Defect
|
Non-Insulin-Dependent Diabetes Of The Young
|
|
Senile Diabetes
|
Nonketotic Hyperglycaemia
|
|
Stable Diabetes
|
|
|
| Peyronie Disease |
|
|
| Amyotrophic Lateral Sclerosis Type 15 |
|
Amyotrophic Lateral Sclerosis 15, With Or Without Frontotemporal Dementia
|
Als15
|
|
Amyotrophic Lateral Sclerosis 15
|
|
|
| Amyotrophic Lateral Sclerosis 21 |
|
Amyotrophic Lateral Sclerosis Type 21
|
ALS21
|
|
Multisystem Proteinopathy 5
|
Msp5
|
|
Distal Myopathy With Vocal Cord Weakness
|
Vcpdm
|
|
Myopathy, Distal, 2, Formerly
|
Mpd2, Formerly
|
|
Vocal Cord And Pharyngeal Dysfunction With Distal Myopathy, Formerly
|
Vcpdm, Formerly
|
|
Vocal Cord And Pharyngeal Distal Myopathy
|
Matr3-Related Distal Myopathy
|
|
Distal Myopathy 2
|
Mpd2
|
|
Vocal Cord And Pharyngeal Dysfunction With Distal Myopathy
|
Sclerosis, Lateral, Amyotrophic, Type 21
|
|
Myopathy, Distal 2
|
|
|
| Hypotonia |
|
|
| Constipation |
|
|
| Postpoliomyelitis Syndrome |
|
Postpolio Syndrome
|
Post-Polio Syndrome
|
|
Post Polio Syndrome
|
Polio Late Effects
|
|
Post-Polio Muscular Atrophy
|
Post-Polio Sequelae
|
|
Post-Poliomyelitic Syndrome
|
Postpolio Sequelae
|
|
Postpoliomyelitic Syndrome
|
Postpoliomyelitis Sequelae
|
|
|
| Viral Hepatitis |
|
Animal Viral Hepatitis
|
Hepatitis, Viral, Animal
|
|
Human Viral Hepatitis
|
Viral Hepatitis With Hepatic Coma
|
|
|
| Dementia |
|
Dementias
|
Presenile Dementia
|
|
Alzheimer Type Dementia
|
Alzheimer Sclerosis
|
|
Alzheimer Disease Dementia
|
Alzheimer Dementia
|
|
Primary Degenerative Alzheimer Type Dementia
|
End Stage Alzheimer'S Dementia
|
|
Alzheimer'S Type Atypical Dementia
|
Alzheimer Type Presenile Dementia
|
|
Early Onset Alzheimer Dementia
|
Dementia In Alzheimer Disease Type 2
|
|
Dementia In Alzheimer Disease With Early Onset
|
Early Onset Alzheimer Type Dementia, Uncomplicated
|
|
Primary Degenerative Alzheimer Type Dementia, Early Onset
|
Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated
|
|
Alzheimer Disease Dementia With Early Onset
|
Presenile Sclerosis
|
|
Presenile Brain Sclerosis
|
Presenile Alzheimer Brain Sclerosis
|
|
Late Onset Alzheimer Dementia
|
Dementia In Alzheimer Disease Type 1
|
|
Dementia In Alzheimer Disease With Late Onset
|
Primary Degenerative Alzheimer Type Dementia, Late Onset
|
|
Sdat - [Senile Dementia, Alzheimer Type]
|
Alzheimer Disease Dementia With Late Onset
|
|
Late Onset Alzheimer Brain Sclerosis
|
Senile Alzheimer Brain Disease
|
|
Senile Alzheimer Brain Sclerosis
|
Senile Primary Degenerative Alzheimer Type Dementia
|
|
Senile Dementia Of The Alzheimer Type
|
Arteriosclerotic Dementia
|
|
Strategic-Infarct Dementia
|
Post Stroke Dementia
|
|
Vascular Cognitive Impairment
|
Vascular Dementia
|
|
Dementia Of The Lewy Body Type
|
Dementia With Lewy Bodies
|
|
Sdlt - [Senile Dementia Of The Lewy Body Type]
|
Senile Dementia Of The Lewy Body Type
|
|
Alcohol-Related Dementia
|
Alcoholic Dementia Nos
|
|
Alcohol-Induced Dementia
|
Alcoholic Brain Syndrome
|
|
Chronic Alcoholic Brain Syndrome
|
Alcohol Dementia
|
|
Late Onset Alcoholic Psychosis
|
Residual And Late-Onset Alcohol-Induced Psychotic Disorder
|
|
Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder
|
Late-Onset Psychoactive Substance-Induced Psychotic Disorder
|
|
Inhalant Dementia
|
Volatile Solvents Dementia
|
|
Dementia In Paralysis Agitans
|
Pdd - [Parkinson Disease Dementia]
|
|
Dementia Syndrome Of Parkinson Disease
|
Dementia In Parkinson Disease
|
|
Parkinson Related Dementia
|
Dementia In Huntington Chorea
|
|
Hiv - [Human Immunodeficiency Virus] Dementia
|
Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex
|
|
Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex
|
Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex
|
|
Aids Related Dementia
|
Dementia Due To Niacin Deficiency
|
|
|
| Platelet Aggregation, Spontaneous |
|
|
| Pseudobulbar Palsy |
|
|
| Alzheimer Disease, Familial, 1 |
|
Alzheimer Disease
|
Alzheimer'S Disease
|
|
Presenile And Senile Dementia
|
AD1
|
|
Alzheimer Disease, Susceptibility To
|
Alzheimer Disease, Late-Onset, Susceptibility To
|
|
Alzheimer Disease 1, Familial
|
AD
|
|
Familial Alzheimer Disease
|
Alzheimer Disease, Late-Onset
|
|
Alzheimers Dementia
|
Alzheimer Dementia
|
|
Alzheimer Sclerosis
|
Alzheimer Syndrome
|
|
Alzheimer-Type Dementia
|
Dat
|
|
Primary Senile Degenerative Dementia
|
Sdat
|
|
Alzheimer Disease 1
|
Autosomal Dominant Alzheimer Disease
|
|
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
|
Late Onset Alzheimer Disease
|
|
Alzheimers Disease
|
Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
|
|
Late-Onset Alzheimers Disease
|
Alzheimer'S Disease Pathway Kegg
|
|
Dementia Due To Alzheimer'S Disease
|
Alzheimer Disease Type 1
|
|
Alzheimers
|
|
|
| Beta-Thalassemia |
|
Beta Thalassemia
|
Cooley'S Anemia
|
|
Mediterranean Anemia
|
Beta Thalassemia Intermedia
|
|
Erythroblastic Anemia
|
Thalassemia, Hispanic Gamma-Delta-Beta
|
|
Thalassemia Major
|
Thalassemia Minor
|
|
Beta-Plus-Thalassemia
|
Thalassemia, Beta
|
|
Beta Thalassemia Major
|
Beta Thalassemia Minor
|
|
Thalassemias, Beta-
|
Microcytemia, Beta Type
|
|
Thalassemia, Beta Type
|
B-THAL
|
|
Mediterranean Anaemia
|
Beta Thalassaemia Syndrome
|
|
Mediterranean Disease
|
Beta Thalassaemia Disease
|
|
|
| Amyotrophic Lateral Sclerosis Type 14 |
|
Als14
|
Amyotrophic Lateral Sclerosis 14
|
|
Amyotrophic Lateral Sclerosis, With Or Without Frontotemporal Dementia
|
Amyotrophic Lateral Sclerosis 14 With Or Without Frontotemporal Dementia
|
|
|
| Glycogen Storage Disease |
|
Glycogenosis
|
Glycogenoses
|
|
Gsd
|
Storage Disease, Glycogen
|
|
Gsd - [Glycogen Storage Disease]
|
Glycogen Thesaurismosis
|
|
Diffuse Glycogenosis
|
Generalised Glycogen Storage Disease
|
|
Generalised Glycogenosis
|
Generalised Glycogen Storage Disease Of Infants
|
|
Glycogen Synthase Deficiency
|
|
|
| Shigellosis |
|
Dysentery, Bacillary
|
Bacillary Dysentery
|
|
Shigella Boydii Infectious Disease
|
Shigella Flexneri Infectious Disease
|
|
Shigella Gastroenteritis
|
Shigella Sonnei Infectious Disease
|
|
Shigella Infections
|
|
|
| Fatal Familial Insomnia |
|
Insomnia, Fatal Familial
|
FFI
|
|
Familial Fatal Insomnia
|
Insomnia Familial Fatal
|
|
Insomnia Fatal Familial
|
Insomnia, Fatal, Familial
|
|
Ffi - [Fatal Familial Insomnia]
|
|
|
| Toxic Encephalopathy |
|
Neurotoxicity
|
Neurotoxicity Syndromes
|
|
Neurotoxicity Syndrome
|
Encephalopathy, Toxic
|
|
|
| Chromosomal Duplication Syndrome |
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Huntington Disease |
|
Huntington'S Disease
|
Huntington Chorea
|
|
Huntington'S Chorea
|
HD
|
|
Huntington Chronic Progressive Hereditary Chorea
|
Juvenile Huntington Disease
|
|
Chronic Progressive Chorea
|
Chronic Progressive Hereditary Chorea
|
|
Hc - [Huntington Chorea]
|
Hereditary Chorea
|
|
Progressive Hereditary Chorea
|
|
|
| Cerebral Palsy |
|
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
|
Palsy Cerebral
|
Palsy, Cerebral
|
|
Cerebral Palsy, Mixed
|
|
|
| Hypertension, Essential |
|
Essential Hypertension
|
Hypertension
|
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
|
Hypertensive Disease
|
Primary Hypertension
|
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
|
Hyperpiesia
|
Idiopathic Hypertension
|
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
|
Htn
|
Vascular Hypertensive Disorder
|
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
|
Arterial Hypertension Nos
|
Hypertension Nos
|
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
|
Systemic Hypertension
|
Artery Htn
|
|
Benign Htn
|
Vascular Htn
|
|
Vascular Hypertension
|
Cholesterol Hypertension
|
|
Cholesterol Htn
|
Idiopathic Htn
|
|
Malignant Hypertension
|
Malignant Htn
|
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
|
Hypertensive Vascular Degeneration
|
|
|
| Short Syndrome |
|
Short Stature, Hyperextensibility, Hernia, Ocular Depression, Rieger Anomaly, And Teething Delay
|
Aarskog-Ose-Pande Syndrome
|
|
Lipodystrophy, Partial, With Rieger Anomaly And Short Stature
|
Lipodystrophy-Rieger Anomaly-Diabetes Syndrome
|
|
Rieger Anomaly-Partial Lipodystrophy Syndrome
|
Partial Lipodystrophy With Rieger Anomaly And Short Stature
|
|
Short Stature, Hyperextensibility, Hernia, Ocular Depression, Rieger Anomaly And Teething Delay
|
Growth Retardation-Rieger Anomaly
|
|
Short Stature-Hyperextensibility-Rieger Anomaly-Teething Delay
|
SHORTS
|
|
|
| Cataract 23, Multiple Types |
|
Cataract 23
|
CTRCT23
|
|
Lamellar Cataract 23
|
Cataract 23, Multiple Types, With Or Without Microcornea
|
|
Isolated Microphthalmia With Cataract 4
|
Mcopct4
|
|
Cataract, Type 23
|
Microphthalmia, Isolated, With Cataract 4
|
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Heart Malformation
|
|
Congenital Anomaly Of Heart
|
Heart Defect
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Pancreatic Colloid Cystadenoma |
|
Mucinous Cystadenoma Of Pancreas
|
|
|
| Chronic Wasting Disease |
|
|
| Anthracosis |
|
Black Lung
|
Coal Workers' Pneumoconiosis
|
|
Melanoedema
|
Black Lung Disease
|
|
Pneumoconiosis
|
Coal Miner'S Pneumoconiosis
|
|
Coal Workers' Lung
|
Coal Worker'S Pneumoconiosis
|
|
Coal Workers Pneumoconiosis
|
Coal Miners' Lung
|
|
Coal Miners' Pneumoconiosis
|
Coal Pneumoconiosis
|
|
Colliers' Anthracosis
|
Colliers' Lung
|
|
Lung Melanosis
|
Miners' Asthma
|
|
Miners' Lung
|
Pneumomelanosis
|
|
Cwp - [Coalworkers Pneumoconiosis]
|
Fibrosis Of Lung With Anthracosilicosis
|
|
Lung Fibrosis With Anthracosis
|
Miners' Pneumoconiosis
|
|
Carbon Lung
|
Coalworker Lung
|
|
Collier'S Asthma
|
Anthracosilicosis
|
|
Lung Anthracosis
|
|
|
| Microvascular Complications Of Diabetes 5 |
|
Diabetic Retinopathy
|
Microvascular Complications Of Diabetes, Susceptibility To, 5
|
|
MVCD5
|
Retinopathy, Diabetic
|
|
Diabetic Nephropathy
|
Retinopathy, Diabetic, Susceptibility To
|
|
Retinal Abnormality - Diabetes-Related
|
|
|
| Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia |
|
Ibmpfd
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia
|
|
Pagetoid Amyotrophic Lateral Sclerosis
|
Pagetoid Neuroskeletal Syndrome
|
|
Inclusion Body Myopathy With Paget Disease Of Bone And/Or Frontotemporal Dementia
|
Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone And/Or Frontotemporal Dementia
|
|
Multisystem Proteinopathy
|
Limb-Girdle Muscular Dystrophy With Paget Disease Of Bone
|
|
Inclusion Body Myopathy With Paget'S Disease Of Bone And Frontotemporal Dementia
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dement
|
|
Lower Motor Neuron Degeneration With Paget-Like Bone Disease
|
Muscular Dystrophy, Limb-Girdle, With Paget Disease Of Bone
|
|
Myopathy, Inclusion Body, With Early-Onset Paget Disease And Frontotemporal Dementia
|
|
|
| Chronic Kidney Disease |
|
Chronic Renal Disease
|
Chronic Kidney Failure
|
|
Ckd
|
Chronic Renal Failure
|
|
Kidney Failure, Chronic
|
Chronic Renal Failure Syndrome
|
|
Crf
|
Renal Failure - Chronic
|
|
Renal Failure Chronic
|
Chronic Kidney Diseases
|
|
Chronic Kidney Disease Stage 5
|
Ckd - [Chronic Kidney Disease]
|
|
Crf - [Chronic Renal Failure]
|
Chronic Kidney Impairment
|
|
Chronic Renal Impairment
|
Chronic Kidney Shutdown
|
|
Chronic Hypoxic Kidney Failure
|
Chronic Kidney Collapse
|
|
Chronic Renal Insufficiency
|
Chronic Kidney Toxaemia
|
|
Chronic Kidney Hypofunction
|
Chronic Renal Suppression
|
|
Chronic Renal Failure, Stage 5
|
Ckd - [Chronic Kidney Disease] Stage 5
|
|
End Stage Kidney Failure
|
End Stage Renal Failure
|
|
End Stage Kidney Disease
|
End Stage Renal Disease
|
|
End Stage Chronic Renal Failure
|
Esrf - [End Stage Renal Failure]
|
|
Esrd - [End Stage Renal Diseases]
|
Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
|
|
|
| Autism Spectrum Disorder |
|
Asd
|
Autism Spectrum Disorders
|
|
Autistic Continuum
|
Pervasive Developmental Disorder
|
|
Pervasive Development Disorder
|
Autistic Behavior
|
|
Autistic Disorder
|
Autistic
|
|
Autistic Disorder Of Childhood Onset
|
Infantile Autism
|
|
Childhood Autism
|
Kanner Syndrome
|
|
Pervasive Developmental Delay Nos
|
Pervasive Developmental Disorder, Not Otherwise Specified
|
|
|
| Malaria |
|
Malaria, Susceptibility To
|
Malaria, Resistance To
|
|
Malaria, Cerebral
|
Cerebral Malaria
|
|
Malaria, Severe, Susceptibility To
|
Malaria, Severe, Resistance To
|
|
Malaria, Cerebral, Susceptibility To
|
Induced Malaria
|
|
Malaria, Vivax, Protection Against
|
Malaria, Severe
|
|
Malaria, Cerebral, Reduced Risk Of
|
Malaria, Protection Against
|
|
Resistance To Malaria Due To G6pd Deficiency
|
Malaria Due To G6pd Deficiency
|
|
Malarial Encephalitis
|
CM
|
|
Malaria Cerebral
|
Susceptibility To Malaria
|
|
Acute Pernicious Fever
|
Aestivo-Autumnal Fever
|
|
Aestivo Autumnal Malaria
|
Chagres Fever
|
|
Continued Malaria Fever
|
Estivo-Autumnal Fever
|
|
Estivo-Autumnal Malaria
|
Estivo-Autumnal Malarial Fever
|
|
Falciparum Fever
|
Malignant Tertian Fever
|
|
Malignant Tertian Malaria
|
Pernicious Intermittent Fever
|
|
Pernicious Malaria
|
Quotidian Malaria
|
|
Subtertian Fever
|
Subtertian Malaria Fever
|
|
Subtertian Malignant Tertian Malaria
|
Tropical Malaria
|
|
Algid Malaria
|
Bilious Haemoglobinuric Fever
|
|
Black Water Fever
|
Blackwater Fever
|
|
Malarial Blackwater Fever
|
Severe Malarial Falciparum
|
|
West African Fever
|
Malarial Haematinuria
|
|
Haemoglobinuric Fever
|
Haemoglobinuric Malaria
|
|
Severe Plasmodium Falciparum Malaria
|
Malarial Haemoglobinuria
|
|
Malarial Haematuria
|
Falciparum Malaria [Malignant Tertian]
|
|
Malaria Tropica
|
Malarial Shock
|
|
Chagres Virus Disease
|
Malignant Malaria
|
|
Mtm - [Malignant Tertian Malaria]
|
Tm -[Malignant Tertian Malaria]
|
|
Panama Fever
|
St - [Subtertian Malaria]
|
|
Malarial Quotidian
|
Benign Tertian Malaria
|
|
Tertian Ague
|
Vivax Fever
|
|
Plasmodium Vivax Malaria Nos
|
Btm - [Benign Tertian Malaria]
|
|
Bt - [Benign Tertian Malaria]
|
Vivax Malaria
|
|
Benign Tertian Vivax Malaria
|
Tertian Malaria
|
|
Quartan Malaria
|
Quartan Ague
|
|
Quartan Fever
|
Plasmodium Malariae Malaria Nos
|
|
Quartan Malarial
|
Malaria By Plasmodium Malariae
|
|
Malariae Malaria
|
Ovale Tertian Malaria
|
|
Plasmodium Ovale Fever
|
Malaria Fever By Plasmodium Ovale
|
|
Ovale Malaria
|
Malaria By Plasmodium Ovale
|
|
Malarial Ovale
|
Marsh Fever
|
|
Remittent Congestive Fever
|
Coastal Fever
|
|
Remittent Gastric Fever
|
Miasmatic Fever
|
|
Congestive Remittent Fever
|
Intermittent Fever
|
|
Jungle Fever
|
Paludism
|
|
Cameroon Fever
|
Ague
|
|
Corsican Fever
|
Intermittent Bilious Fever
|
|
Disease Due To Plasmodiidae
|
Malarial Fever
|
|
Plasmodiosis
|
Remittent Fever
|
|
Roman Fever
|
Malaria Fever Nos
|
|
Malaria Nos
|
Paludal Fever
|
|
Clinically Diagnosed Malaria
|
Clinically Diagnosed Malaria Without Parasitological Confirmation
|
|
Congestive Fever
|
Malarial Cachexia
|
|
Marsh Cachexia
|
Paludal Cachexia
|
|
Recurrent Malaria
|
Remittent Malaria
|
|
|
| Dementia, Lewy Body |
|
Lewy Body Dementia
|
Lewy Body Disease
|
|
Diffuse Lewy Body Disease
|
Dementia With Lewy Bodies
|
|
DLB
|
Autosomal Dominant Diffuse Lewy Body Disease
|
|
Cortical Lewy Body Disease
|
Dementia, Lewy Body, Susceptibility To
|
|
Lewy Body Dementia, Susceptibility To
|
Senile Dementia Of The Lewy Body Type
|
|
Dementia Of The Lewy Body Type
|
Lbd
|
|
Diffuse Lewy Body Disease With Gaze Palsy
|
Dysphasic Dementia Hereditary
|
|
Lewy Body Type Senile Dementia
|
Lewy Body Variant Of Alzheimer Disease
|
|
Lewy Bodies
|
Lewy Body
|
|
Dlbd - [Diffuse Lewy Body Disease]
|
Clbd - [Cortical Lewy Body Disease]
|
|
|
| Pick Disease Of Brain |
|
Pick Disease
|
Pick'S Disease
|
|
Pick Disease Of The Brain
|
Lobar Atrophy Of Brain
|
|
Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions
|
Behavioral Variant Of Frontotemporal Dementia
|
|
Dementia In Pick'S Disease
|
Lobar Atrophy Of The Brain
|
|
Bvftd
|
Bv-Ftd
|
|
PIDB
|
Picks Disease
|
|
|
| Neuroblastoma |
|
Nb
|
Neuroblastoma, Susceptibility To
|
|
Neuroblastomas
|
Central Neuroblastoma
|
|
|
| Pheochromocytoma |
|
Pheochromocytoma, Susceptibility To
|
Phaeochromocytoma
|
|
Adrenal Gland Chromaffin Paraganglioma
|
Adrenal Gland Chromaffinoma
|
|
Adrenal Gland Paraganglioma
|
Adrenal Gland Pheochromocytoma
|
|
Chromaffin Paraganglioma Of The Adrenal Gland
|
Intraadrenal Paraganglioma
|
|
PCC
|
Chromaffin Cell Tumor
|
|
Medullary Chromaffinoma
|
Medullary Paraganglioma
|
|
Pheochromoblastoma
|
Pheochromocytomas
|
|
Chromaffin Cell Neoplasm
|
Pheochromocytoma, Malignant
|
|
|
| Hereditary Ataxia |
|
Sca
|
Spinocerebellar Ataxia
|
|
Ataxias Hereditary
|
Ataxias, Hereditary
|
|
|
| Autosomal Dominant Cerebellar Ataxia |
|
Spinocerebellar Ataxia
|
Adca
|
|
Pierre Marie Cerebellar Ataxia
|
Ataxia, Spinocerebellar
|
|
Sca
|
Autosomal Dominant Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxias
|
|
|
| Spastic Paraplegia 38, Autosomal Dominant |
|
SPG38
|
Hereditary Spastic Paraplegia 38
|
|
Autosomal Dominant Spastic Paraplegia Type 38
|
Autosomal Dominant Spastic Paraplegia 38
|
|
|
| Supranuclear Palsy, Progressive, 1 |
|
Progressive Supranuclear Palsy
|
Steele-Richardson-Olszewski Syndrome
|
|
Supranuclear Palsy, Progressive
|
Progressive Supranuclear Ophthalmoplegia
|
|
Psp
|
PSNP1
|
|
Familial Progressive Supranuclear Palsy
|
Richardson'S Syndrome
|
|
Psp Syndrome
|
Progressive Supranuclear Palsy 1
|
|
Supranuclear Palsy Progressive
|
Ophthalmoplegia, Supranuclear, Progressive
|
|
Steele-Richardson-Olszewksi Syndrome
|
|
|
| Tetralogy Of Fallot |
|
TOF
|
Fallot Tetralogy
|
|
Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle
|
Tetrad Of Fallot
|
|
Fallot Tetrad
|
Fallot Disease
|
|
Fallot Complex
|
Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy
|
|
Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle
|
Interventricular Septal Defect, In Tetralogy Of Fallot
|
|
Ventricular Septal Defect With Obstructed Right Ventricular Outflow
|
Tof - [Tetralogy Of Fallot]
|
|
Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]
|
Pulmonary Atresia, Ventricular Septal Defect And Mapcas
|
|
Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
|
|
|
| Cerebellar Disease |
|
Cerebellar Diseases
|
Cerebellar Dysfunction
|
|
Cerebellar Abnormality
|
Cerebellar Disorders
|
|
|
| Alzheimer Disease 9 |
|
AD9
|
Alzheimer'S Disease 9
|
|
Alzheimer Disease 9, Susceptibility To
|
Alzheimer Disease 9, Late-Onset
|
|
Alzheimer'S Disease 9, Late Onset
|
{Alzheimer Disease 9, Susceptibility To}
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| Scoliosis |
|
|
| Spinal Muscular Atrophy, Type I |
|
Werdnig-Hoffmann Disease
|
SMA1
|
|
Spinal Muscular Atrophy 1
|
Sma I
|
|
Sma, Infantile Acute Form
|
Muscular Atrophy, Infantile
|
|
Spinal Muscular Atrophy-1
|
Hmn Proximal Type I
|
|
Infantile Muscular Atrophy
|
Proximal Spinal Muscular Atrophy Type 1
|
|
Sma Type 1
|
Sma Type I
|
|
Sma-I
|
Hereditary Motor Neuropathy Proximal Type I
|
|
Progressive Muscular Atrophy Of Infancy
|
Proximal Spinal Muscular Atrophy, Type 1
|
|
Werdnig Hoffmann Disease
|
Infantile Spinal Muscular Atrophy
|
|
Infantile-Onset Spinal Muscular Atrophy
|
Proximal Hereditary Motor Neuropathy Type I
|
|
Sma Infantile Acute Form
|
Spinal Muscular Atrophy Type I
|
|
Werdnig-Hoffman Disease
|
Atrophy, Muscular, Spinal, Type 1
|
|
|
| Autism |
|
Autistic Disorder
|
Autism Susceptibility 1
|
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
|
Infantile Autism
|
Kanner'S Syndrome
|
|
Autistic
|
|
|
| Movement Disease |
|
Movement Disorders
|
Movement Disorder
|
|
|
| Giant Axonal Neuropathy 2 |
|
|
| Choreatic Disease |
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Hereditary Spastic Paraplegia |
|
Familial Spastic Paraplegia
|
Hereditary Spastic Paraparesis
|
|
Strumpell-Lorrain Disease
|
Familial Spastic Paraparesis
|
|
Hsp
|
Spg
|
|
Strümpell-Lorrain Disease
|
Spastic Paraplegia, Hereditary
|
|
French Settlement Disease
|
Strumpell-Lorrain Syndrome
|
|
Fsp
|
Spastic Paraplegia, Familial
|
|
Spastic Paraplegia Hereditary
|
Spastic Paraplegia 3, Autosomal Dominant
|
|
Spastic Paraparesis
|
Hereditary Spastic Paralysis
|
|
Familial Spastic Paralysis
|
Hereditary Spastic Ataxia
|
|
|
| Respiratory Failure |
|
Acute Respiratory Failure
|
Chronic Respiratory Failure
|
|
Respiratory Insufficiency
|
Acute-On-Chronic Respiratory Failure
|
|
Respiratory Disease
|
Acute And Chronic Respiratory Failure
|
|
Respiratory Insufficiency/Failure
|
Chronic Respiratory Disease
|
|
Pulmonary Valve Insufficiency
|
Chronic Disease Of Respiratory System
|
|
Respiration Disorders
|
Respiratory Tract Diseases
|
|
Lung Failure Nos
|
Pulmonary Failure
|
|
Arf - [Acute Respiratory Failure]
|
Acute Respiratory Insufficiency
|
|
Acute Pulmonary Insufficiency
|
Acute Respiration Failure
|
|
Chronic Respiration Failure
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| Neuronal Ceroid Lipofuscinosis |
|
Hereditary Ceroid Lipofuscinosis
|
Batten Disease
|
|
Ncl
|
Neuronal Ceroid-Lipofuscinoses
|
|
Lipofuscinosis, Ceroid, Neuronal
|
Juvenile Neuronal Ceroid Lipofuscinosis
|
|
Cerebromacular Dystrophy
|
Cerebromacular Degeneration
|
|
Ceroid-Lipofuscinosis
|
Ncl - [Neuronal Ceroid Lipofuscinosis]
|
|
Amaurotic Familial Idiocy
|
Amaurotic Idiocy
|
|
Amaurotic Idiot
|
Neuronal Lipofuscinosis
|
|
Pigmentary Retinal Lipoid Neuronal Heredodegeneration
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
