| 疾病名称 |
别名 |
|
| Neuropathy, Hereditary Sensory And Autonomic, Type Iia |
|
Hereditary Sensory And Autonomic Neuropathy Type 2
|
Hsan2
|
|
HSAN2A
|
Morvan Disease
|
|
Hereditary Sensory And Autonomic Neuropathy Type Ii
|
Neurogenic Acroosteolysis
|
|
Hsan Iia
|
Hsn2a
|
|
Hsn Iia
|
Neuropathy, Progressive Sensory, Of Children
|
|
Neuropathy, Congenital Sensory
|
Neuropathy, Hereditary Sensory And Autonomic, Type Ii
|
|
Hereditary Sensory And Autonomic Neuropathy Type 2a
|
Hereditary Sensory And Autonomic Neuropathy Type Iia
|
|
Hsanii
|
Congenital Sensory Neuropathy
|
|
Hsan Type Ii
|
Morvan Syndrome
|
|
Neuropathy, Hereditary Sensory And Autonomic, Type 2a
|
Morvan'S Disease
|
|
Neuropathy, Hereditary Sensory, Type Iia
|
Acroosteolysis, Neurogenic
|
|
Acroosteolysis, Giaccai Type
|
Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive
|
|
Hereditary Sensory Autonomic Neuropathy Type 2
|
Giaccai Type Acroosteolysis
|
|
Hereditary Sensory Neuropathy Type 2
|
Hereditary Sensory Radicular Neuropathy, Recessive Form
|
|
Hsan2b
|
Hsan2c
|
|
Hsan2d
|
Hsn Type Ii
|
|
Autosomal Recessive Sensory Radicular Neuropathy
|
Limbic Encephalitis-Neuromyotonia-Hyperhidrosis-Polyneuropathy Syndrome
|
|
Morvan Fibrillary Chorea
|
Neuropathy, Hereditary Sensory And Autonomic, 2a
|
|
Acroosteolysis Giaccai Type
|
Hereditary Sensory Neuropathy Type Iia
|
|
Hereditary Sensory Radicular Neuropathy Autosomal Recessive
|
Progressive Sensory Neuropathy Of Children
|
|
Neuropathy Congenital Sensory
|
Charcot-Marie-Tooth Disease
|
|
Neuropathy, Sensory And Autonomic, Hereditary, Type Iia
|
Hereditary Sensory Autonomic Neuropathy, Type 2
|
|
Hereditary Motor And Sensory-Neuropathy Type Ii
|
Sensory Neuropathy, Hereditary
|
|
Neuropathy, Hereditary Sensory And Autonomic, Type Iib
|
|
|
| Arthrogryposis, Distal, Type 3 |
|
Gordon Syndrome
|
DA3
|
|
Distal Arthrogryposis Type 3
|
Arthrogryposis Multiplex Congenita, Distal, Type Iia
|
|
Camptodactyly, Cleft Palate, And Clubfoot
|
Camptodactyly-Cleft Palate-Clubfoot Syndrome
|
|
Distal Arthrogryposis Multiplex Congenita Type Iia
|
Arthrogryposis Distal Type 3
|
|
Distal Arthrogryposis Type Iia
|
Arthrogryposis, Distal, 3
|
|
Pseudohypoaldosteronism, Type Ii
|
|
|
| Gitelman Syndrome |
|
Familial Hypokalemia-Hypomagnesemia
|
Hypomagnesemia-Hypokalemia, Primary Renotubular, With Hypocalciuria
|
|
Potassium And Magnesium Depletion
|
GTLMNS
|
|
Gitelman'S Syndrome
|
Gs
|
|
Hypokalemia-Hypomagnesemia, Primary Renotubular, With Hypocalciuria
|
Tubular Hypomagnesemia-Hypokalemia With Hypocalcuria
|
|
Bartter Syndrome Gitelman Variant
|
Bartter Syndrome Hypocalciuric Variant
|
|
Primary Renotubular Hypomagnesemia-Hypokalemia With Hypocalciuria
|
|
|
| Agenesis Of The Corpus Callosum With Peripheral Neuropathy |
|
Andermann Syndrome
|
Charlevoix Disease
|
|
ACCPN
|
Polyneuropathy, Sensorimotor, With Or Without Agenesis Of The Corpus Callosum
|
|
Corpus Callosum, Agenesis Of, With Neuronopathy
|
Corpus Callosum Agenesis-Neuronopathy Syndrome
|
|
Agenesis Of Corpus Callosum With Neuronopathy
|
Agenesis Of Corpus Callosum With Peripheral Neuropathy
|
|
Agenesis Of Corpus Callosum With Polyneuropathy
|
Corpus Callosum Agenesis Neuronopathy
|
|
Hmsn/Acc
|
Hereditary Motor And Sensory Neuropathy With Agenesis Of The Corpus Callosum
|
|
Agenesis Of The Corpus Callosum, With Peripheral Neuropathy
|
Andermann'S Syndrome
|
|
Agenesis, Corpus Callosum, With Peripheral Neuropathy
|
|
|
| Renal Tubular Transport Disease |
|
Renal Tubular Transport, Inborn Errors
|
Inborn Renal Tubular Transport Disorder
|
|
|
| Developmental And Epileptic Encephalopathy 34 |
|
DEE34
|
Epileptic Encephalopathy, Early Infantile, 34
|
|
Eiee34
|
Developmental And Epileptic Encephalopathy, 34
|
|
Early Infantile Epileptic Encephalopathy 34
|
|
|
| Pseudohypoaldosteronism |
|
|
| Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, And Electrolyte Imbalance |
|
Sesame Syndrome
|
East Syndrome
|
|
SESAMES
|
Epilepsy, Ataxia, Sensorineural Deafness And Tubulopathy
|
|
Seizures, Sensorineural Deafness, Ataxia, Mental Retardation And Electrolyte Imbalance
|
Epilepsy-Ataxia-Sensorineural Deafness-Tubulopathy Syndrome
|
|
Seizures-Sensorineural Deafness-Ataxia-Intellectual Disability-Electrolyte Imbalance Syndrome
|
Epilepsy, Ataxia, Sensorineural Deafness, And Tubulopathy
|
|
Seizures - Sensorineural Deafness - Ataxia - Intellectual Disability - Electrolyte Imbalance
|
Epilepsy-Ataxia-Sensorineural Hearing Loss-Tubulopathy Syndrome
|
|
Seizures-Sensorineural Hearing Loss-Ataxia-Intellectual Disability-Electrolyte Imbalance Syndrome
|
Seizures, Sensorineural Deafness, Ataxia, Intellectual Disability, And Electrolyte Imbalance
|
|
Epilepsy Ataxia Sensorineural Deafness And Tubulopathy
|
Seizures, Sensorineural Deafness, Ataxia, Intellectual Disability, And Electrolyte Imbalance Syndrome
|
|
|
| Bartter Disease |
|
Bartter Syndrome
|
Bartter'S Syndrome
|
|
Aldosteronism With Hyperplasia Of The Adrenal Cortex
|
Hypokalemic Alkalosis With Hypercalciuria
|
|
Potassium Wasting
|
Juxtaglomerular Hyperplasia With Secondary Aldosteronism
|
|
Renal Tubular Normotensive Hypokalemic Alkalosis With Hypercalciuria
|
Salt-Losing Tubular Disorder, Henle'S Loop Type
|
|
Salt-Wasting Tubulopathy, Henle'S Loop Type
|
Bartters Syndrome
|
|
|
| Meier-Gorlin Syndrome 2 |
|
MGORS2
|
Meier-Gorlin Syndrome, Type 2
|
|
|
| Epilepsy, Idiopathic Generalized 9 |
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 9
|
EIG9
|
|
Epilepsy, Juvenile Myoclonic 6
|
Idiopathic Generalized Epilepsy 9
|
|
Epilepsy, Juvenile Myoclonic, Susceptibility To, 6
|
Susceptibility To Idiopathic Generalized Epilepsy 9
|
|
Juvenile Myoclonic Epilepsy 6
|
EJM6
|
|
Susceptibility To Juvenile Myoclonic Epilepsy 6
|
Epilepsy, Idiopathic, Generalized, Susceptibility To, Type 9
|
|
|
| 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
|
|
|
| Liddle Syndrome 1 |
|
Liddle Syndrome
|
Pseudoaldosteronism
|
|
Liddle'S Syndrome
|
LIDLS1
|
|
Lidls
|
Pseudohyperaldosteronism
|
|
Pseudoprimary Hyperaldosteronism
|
Pseudohyperaldosteronism Type 1
|
|
Liddles Syndrome
|
|
|
| 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
|
|
|
| Distal Arthrogryposis |
|
Arthrogryposis Multiplex Congenita
|
Arthrogryposis
|
|
Congenital Multiple Arthrogryposis
|
Congenital Arthromyodysplasia
|
|
Fibrous Ankylosis Of Multiple Joints
|
Guerin-Stern Syndrome
|
|
Guérin-Stern Syndrome
|
Myodystrophia Fetalis Deformans
|
|
Otto Syndrome
|
Rocher-Sheldon Syndrome
|
|
Rossi Syndrome
|
Amc
|
|
Multiple Congenital Arthrogryposis
|
Arthrogryposis Syndrome
|
|
Arthrogryposis, Distal
|
Distal Arthrogryposis Syndrome
|
|
Freeman-Sheldon Syndrome
|
Arthrogryposis, Distal, Type 2b
|
|
Congenital Multiplex Arthrogryposis
|
Amyoplasia Congenita
|
|
Congenital Amyoplasia
|
Amc - [Arthrogryposis Multiplex Congenita]
|
|
|
