| 疾病名称 |
别名 |
|
| Influenza |
|
Flu
|
Influenza With Non-Respiratory Manifestation
|
|
Influenza With Other Manifestations
|
Influenza, Human
|
|
Influenza, Susceptibility To
|
Seasonal Influenza, Virus Identified
|
|
|
| Myeloperoxidase Deficiency |
|
|
| Nephrogenic Diabetes Insipidus |
|
Vasopressin-Resistant Diabetes Insipidus
|
Diabetes Insipidus, Nephrogenic
|
|
Diabetes Insipidus Nephrogenic
|
Congenital Nephrogenic Diabetes Insipidus
|
|
Adh Resistant Diabetes Insipidus
|
Diabetes Insipidus Nephrogenic X-Linked
|
|
Diabetes Insipidus Nephrogenic Type 1
|
Adh-Resistant Diabetes Insipidus
|
|
Diabetes Insipidus Renalis
|
Ndi
|
|
Renal Diabetes Insipidus
|
Familial Nephrogenic Diabetes
|
|
Antidiuretic-Hormone-Resistant Diabetes Insipidus
|
Adiuretin-Resistant Diabetes Insipidus
|
|
Ndi - [Nephrogenic Diabetes Insipidus]
|
Diabetes Tenuifluus
|
|
Adh - [Antidiuretic-Hormone] Resistant Diabetes Insipidus
|
Hereditary Nephrogenic Diabetes Insipidus
|
|
Familial Nephrogenic Diabetes Insipidus
|
Primary Nephrogenic Diabetes Insipidus
|
|
|
| Pseudoachondroplasia |
|
PSACH
|
Pseudoachondroplastic Dysplasia
|
|
Pseudoachondroplastic Spondyloepiphyseal Dysplasia Syndrome
|
Spondyloepiphyseal Dysplasia, Pseudoachondroplastic
|
|
Pseudoachondroplastic Spondyloepiphyseal Dysplasia
|
Spondyloepiphyseal Dysplasia Pseudoachondroplastic
|
|
|
| Cystic Fibrosis |
|
Mucoviscidosis
|
CF
|
|
Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis
|
Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis
|
|
Cystic Fibrosis Lung Disease, Modifier Of
|
Cystic Fibrosis Of Pancreas
|
|
Fibrocystic Disease Of Pancreas
|
Cf - [Cystic Fibrosis]
|
|
Cystic Fibrosis Nos
|
Fibrocystic Disease
|
|
Fibrocystic Disease Of The Pancreas
|
Mucoviscidosis Of Pancreas
|
|
Nonproliferative Fibrocystic Disease
|
Pancreatic Cystic Fibrosis
|
|
|
| Oculocutaneous Albinism |
|
Albinism, Oculocutaneous
|
Oca
|
|
Albinism Oculocutaneous
|
Oca - [Oculocutaneous Albinism]
|
|
|
| Lipase Deficiency, Combined |
|
Lipoprotein Lipase Deficiency With Hepatic Triglyceride Lipase Deficiency
|
Lpl And Htgl Deficiency
|
|
Lpl And Hl Deficiency
|
Familial Lipase Maturation Factor 1 Deficiency
|
|
Lipase Deficiency Combined
|
Combined Lipase Deficiency
|
|
Familial Lmf1 Deficiency
|
CLD
|
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt Syndrome
|
|
|
| Congenital Disorder Of Glycosylation, Type Iib |
|
CDG2B
|
CDGIIB
|
|
Glucosidase I Deficiency
|
Congenital Disorder Of Glycosylation Type Iib
|
|
Cdg Iib
|
Mogs-Cdg
|
|
Cdg Syndrome Type Iib
|
Cdg-Iib
|
|
Carbohydrate Deficient Glycoprotein Syndrome Type Iib
|
Congenital Disorder Of Glycosylation Type 2b
|
|
Glucosidase 1 Deficiency
|
Type Iib Congenital Disorder Of Glycosylation
|
|
Glycosylation, Congenital Disorder Of, Type Iib
|
|
|
| Mast Cell Neoplasm |
|
Mastocytoma
|
Mast Cell Proliferative Disease
|
|
Mast Cell Tumor
|
Benign Mastocytoma
|
|
|
| Retinitis Pigmentosa 77 |
|
RP77
|
Retinitis Pigmentosa, Type 77
|
|
|
| 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
|
|
|
| Charcot-Marie-Tooth Disease And Deafness |
|
Charcot-Marie-Tooth Disease Type 1e
|
CMT1E
|
|
Charcot-Marie-Tooth Disease Type 1
|
Hereditary Motor And Sensory Neuropathy Type 1
|
|
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e
|
Charcot-Marie-Tooth Disease, Type I
|
|
Charcot-Marie-Tooth Neuropathy And Deafness, Autosomal Dominant
|
Charcot-Marie-Tooth Disease, Type 1e
|
|
Charcot-Marie-Tooth Disease Demyelinating Type 1e
|
Autosomal Dominant Demyelinating Charcot-Marie-Tooth Disease
|
|
Cmt1
|
Charcot-Marie-Tooth Neuropathy Type 1
|
|
Autosomal Dominant Charcot-Marie-Tooth Neuropathy And Deafness
|
Charcot-Marie-Tooth Disease-Deafness
|
|
Charcot-Marie-Tooth Type 1
|
Hmsn1
|
|
Hereditary Motor And Sensory Neuropathy 1
|
Cmt 1e
|
|
Charcot Marie Tooth Disease Type 1e
|
Charcot-Marie-Tooth Disease-Deafness Syndrome
|
|
Charcot-Marie-Tooth Disease-Hearing Loss Syndrome
|
Charcot-Marie-Tooth Disease 1e
|
|
Charcot-Marie-Tooth Disease And Deafness Autosomal Dominant
|
Charcot-Marie-Tooth Neuropathy Type 1e
|
|
Charcot-Marie-Tooth Disease, Type Ie
|
Hereditary Motor And Sensory Neuropathy Type I
|
|
|
| Legionnaire Disease |
|
Legionnaires' Disease
|
Legionnaires Disease
|
|
Legionnaire Disease, Susceptibility To
|
Legionella
|
|
Legionella Pneumonia
|
Infection By Legionella Pneumophilia
|
|
Legionnaire'S Disease
|
Legionellosis
|
|
Legionaire Disease, Susceptibility To
|
Legionnaires Pneumonia
|
|
|
| Legionellosis |
|
Legionella Infection
|
Pontiac Fever
|
|
Legionnaires' Disease
|
Infection By Legionella Pneumophilia
|
|
Legionella Pneumophila Infection
|
|
|
| Marfan Syndrome |
|
MFS
|
Mfs1
|
|
Marfan'S Syndrome
|
Marfan Syndrome Type 1
|
|
Marfan Syndrome, Type I
|
Mass Phenotype
|
|
Contractural Arachnodactyly
|
Mass Syndrome
|
|
Octd
|
Overlap Connective Tissue Disease
|
|
Marfanoid Hypermobility Syndrome
|
Marfan Disease
|
|
|
| Dystonia |
|
Dystonic Disease
|
Dystonic Disorder
|
|
Dystonia Disorders
|
Neuroleptic Dyskinesia
|
|
|
| Esophageal Adenosquamous Carcinoma |
|
|
| Hypertrophic Neuropathy Of Dejerine-Sottas |
|
Dejerine-Sottas Disease
|
Dejerine-Sottas Syndrome
|
|
Charcot-Marie-Tooth Disease Type 3
|
DSS
|
|
Hereditary Motor And Sensory Neuropathy Type Iii
|
Hmsn3
|
|
Dejerine-Sottas Neuropathy
|
Hmsn Iii
|
|
Charcot-Marie-Tooth Disease, Type 3
|
Cmt3
|
|
Dsn
|
Hmsn 3
|
|
Hereditary Motor And Sensory Neuropathy Type 3
|
Hereditary Motor And Sensory Neuropathy 3
|
|
Hypertrophic Neuropathy Of Infancy
|
Charcot-Marie-Tooth Disease Demyelinating Type 4f
|
|
Charcot-Marie-Tooth Disease Type 4f
|
Charcot-Marie-Tooth Neuropathy Type 4f
|
|
Cmt4f
|
Hereditary Motor And Sensory Neuropathy Iii
|
|
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
|
|
|
| Long Qt Syndrome 2 |
|
LQT2
|
Long Qt Syndrome, Acquired, Reduced Susceptibility To
|
|
Long Qt Syndrome 1/2
|
Long Qt Syndrome 2/3
|
|
Long Qt Syndrome 2/5
|
Long Qt Syndrome 2, Acquired, Susceptibility To
|
|
Long Qt Syndrome, Acquired, Reduced
|
Long Qt Syndrome Type 2
|
|
Long Qt Syndrome 2/9
|
Lqt1/2
|
|
Lqt2/3
|
Lqt2/5
|
|
Lqt2/9
|
Susceptibility To Acquired Long Qt Syndrome 2
|
|
Long Qt Syndrome-2
|
Qt Syndrome, Long, Type 2
|
|
Long Qt Syndrome 1-2
|
Long Qt Syndrome 2-3
|
|
Long Qt Syndrome 2-5
|
Long Qt Syndrome 9
|
|
|
| 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
|
|
|
| Congenital Disorder Of Glycosylation, Type In |
|
Congenital Disorder Of Glycosylation
|
CDG1N
|
|
Congenital Disorders Of Glycosylation
|
Cdg In
|
|
Cdgin
|
Congenital Disorder Of Glycosylation 1n
|
|
Carbohydrate-Deficient Glycoprotein Syndrome
|
Cdg
|
|
Rft1-Cdg
|
Cdg-In
|
|
Congenital Disorder Of Glycosylation Type In
|
Carbohydrate Deficient Glycoprotein Syndrome
|
|
Cdg Syndrome
|
Congenital Disorder Of Glycosylation In
|
|
Carbohydrate-Deficient Glycoprotein Syndromes
|
Cdg Syndrome Type In
|
|
Carbohydrate Deficient Glycoprotein Syndrome Type In
|
Congenital Disorder Of Glycosylation Type 1n
|
|
Man5glcnac2-Pp-Dol Flippase Deficiency
|
Glycosylation, Congenital Disorder Of
|
|
Glycosylation, Congenital Disorder Of, Type In
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
