| 疾病名称 |
别名 |
|
| Deafness, Autosomal Dominant 2a |
|
DFNA2A
|
Autosomal Dominant Nonsyndromic Deafness 2a
|
|
Autosomal Dominant Deafness 2a
|
Deafness, Autosomal Dominant, 2a
|
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 2a
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 2a
|
|
Deafness, Autosomal Dominant, Type 2a
|
|
|
| Dfna2 Nonsyndromic Hearing Loss |
|
Dfna 2 Nonsyndromic Hearing Loss
|
|
|
| Non-Syndromic Genetic Deafness |
|
Nonsyndromic Genetic Hearing Loss
|
Isolated Genetic Deafness
|
|
Isolated Genetic Hearing Loss
|
Non-Syndromic Genetic Hearing Loss
|
|
|
| Nonsyndromic Hearing Loss |
|
Nonsyndromic Deafness
|
Nonsyndromic Hearing Impairment
|
|
Nonsyndromic Hearing Loss And Deafness
|
Deafness, Nonsyndromic
|
|
Isolated Deafness
|
|
|
| Rare Genetic Deafness |
|
Rare Genetic Hearing Loss
|
|
|
| Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna |
|
Autosomal Dominant Isolated Neurosensory Deafness Type Dfna
|
Autosomal Dominant Isolated Neurosensory Hearing Loss Type Dfna
|
|
Autosomal Dominant Isolated Sensorineural Deafness Type Dfna
|
Autosomal Dominant Isolated Sensorineural Hearing Loss Type Dfna
|
|
Autosomal Dominant Non-Syndromic Neurosensory Deafness Type Dfna
|
Autosomal Dominant Non-Syndromic Neurosensory Hearing Loss Type Dfna
|
|
Autosomal Dominant Non-Syndromic Sensorineural Hearing Loss Type Dfna
|
|
|
| Sensorineural Hearing Loss |
|
Sensory Hearing Loss
|
Sensorineural Deafness
|
|
Sensorineural Hearing Loss Disorder
|
Hearing Loss, Sensorineural
|
|
Central Hearing Loss
|
High Frequency Deafness
|
|
High Frequency Hearing Loss
|
High-Frequency Hearing Loss
|
|
Perceptive Deafness
|
Perceptive Hearing Loss
|
|
Perceptive Hearing Loss Or Deafness
|
Hearing Loss Sensorineural
|
|
Deafness Sensorineural
|
Hearing Loss High-Frequency
|
|
Hearing Loss, Central
|
Hearing Loss, High-Frequency
|
|
|
| Deafness, Autosomal Dominant 18 |
|
DFNA18
|
Autosomal Dominant Nonsyndromic Deafness 18
|
|
Autosomal Dominant Deafness 18
|
|
|
| Deafness, Autosomal Dominant 15 |
|
DFNA15
|
Autosomal Dominant Nonsyndromic Deafness 15
|
|
Autosomal Dominant Deafness 15
|
Deafness, Autosomal Dominant, 15
|
|
Deafness, Autosomal Dominant, Type 15
|
|
|
| Deafness, Autosomal Dominant 9 |
|
DFNA9
|
Autosomal Dominant Nonsyndromic Deafness 9
|
|
Autosomal Dominant Deafness 9
|
Deafness, Autosomal Dominant, 9
|
|
Deafness, Autosomal Dominant, Type 9
|
|
|
| Benign Neonatal Seizures |
|
Benign Neonatal Epilepsy
|
Benign Familial Neonatal Seizures
|
|
Benign Neonatal Convulsions
|
Benign Familial Neonatal Convulsions
|
|
Benign Familial Neonatal Epilepsy
|
Bfne
|
|
Bfns
|
Seizures, Benign Neonatal
|
|
Neonatal Convulsions Benign
|
Epilepsy, Benign Neonatal
|
|
Epilepsy, Benign Neonatal, 2
|
Benign Familial Convulsion
|
|
Familial Benign Neonatal Epilepsy
|
|
|
| Deafness, Autosomal Dominant 25 |
|
DFNA25
|
Autosomal Dominant Nonsyndromic Deafness 25
|
|
Autosomal Dominant Deafness 25
|
Deafness, Autosomal Dominant, 25
|
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 25
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 25
|
|
Deafness, Autosomal Dominant, Type 25
|
|
|
| Deafness, Autosomal Dominant 28 |
|
DFNA28
|
Autosomal Dominant Nonsyndromic Deafness 28
|
|
Autosomal Dominant Deafness 28
|
Deafness, Autosomal Dominant, 28
|
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 28
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 28
|
|
Deafness, Autosomal Dominant, Type 28
|
|
|
| Deafness, Autosomal Recessive 14 |
|
DFNB14
|
Autosomal Recessive Nonsyndromic Deafness 14
|
|
Autosomal Recessive Deafness 14
|
|
|
| Deafness, Autosomal Dominant 2b |
|
DFNA2B
|
Autosomal Dominant Nonsyndromic Deafness 2b
|
|
Autosomal Dominant Deafness 2b
|
Deafness, Autosomal Dominant, 2b
|
|
Deafness, Autosomal Dominant, Type 2b
|
|
|
| Deafness, Autosomal Dominant 13 |
|
DFNA13
|
Autosomal Dominant Nonsyndromic Deafness 13
|
|
Autosomal Dominant Deafness 13
|
Deafness, Autosomal Dominant, 13
|
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 13
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 13
|
|
Deafness, Autosomal Dominant, Type 13
|
|
|
| Deafness, Autosomal Dominant 44 |
|
DFNA44
|
Autosomal Dominant Nonsyndromic Deafness 44
|
|
Autosomal Dominant Deafness 44
|
Deafness, Autosomal Dominant, 44
|
|
Deafness, Autosomal Dominant, Type 44
|
|
|
| Deafness, Autosomal Dominant 41 |
|
DFNA41
|
Autosomal Dominant Nonsyndromic Deafness 41
|
|
Autosomal Dominant Deafness 41
|
Deafness, Autosomal Dominant, 41
|
|
Deafness, Autosomal Dominant, Type 41
|
|
|
| Superior Semicircular Canal Dehiscence |
|
Superior Canal Dehiscence Syndrome
|
Superior Semicircular Canal Dehiscence Syndrome
|
|
Canal Dehiscence Syndrome
|
Superior Canal Dehiscence
|
|
Superior Canal Syndrome
|
Third Mobile Window Syndrome
|
|
Scds
|
Anemia, Sickle Cell
|
|
|
| Deafness, Autosomal Dominant 16 |
|
DFNA16
|
Autosomal Dominant Nonsyndromic Deafness 16
|
|
Autosomal Dominant Deafness 16
|
|
|
| Deafness, Autosomal Recessive 4, With Enlarged Vestibular Aqueduct |
|
Enlarged Vestibular Aqueduct
|
DFNB4
|
|
Neurosensory Nonsyndromic Recessive Deafness 4
|
Enlarged Vestibular Aqueduct Syndrome
|
|
Nsrd4
|
Autosomal Recessive Nonsyndromic Deafness 4
|
|
Dilated Vestibular Aqueduct
|
Dva
|
|
Enlarged Vestibular Aqueduct, Digenic
|
Autosomal Recessive Deafness 4 With Enlarged Vestibular Aqueduct
|
|
Large Vestibular Aqueduct Syndrome
|
Deafness, Autosomal Recessive, 4
|
|
Deafness Neurosensory Autosomal Recessive 4
|
Eva
|
|
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 4
|
Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 4
|
|
Deafness, Autosomal Recessive, Type 4 , With Enlarged Vestibular Aqueduct
|
|
|
| Deafness, Autosomal Dominant 10 |
|
DFNA10
|
Autosomal Dominant Nonsyndromic Deafness 10
|
|
Autosomal Dominant Deafness 10
|
Deafness, Autosomal Dominant, 10
|
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 10
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 10
|
|
Deafness, Autosomal Dominant, Type 10
|
|
|
| Waardenburg Syndrome, Type 4c |
|
Waardenburg Syndrome Type 4c
|
WS4C
|
|
Waardenburg Syndrome Type Ivc
|
Waardenburg Syndrome With Hirschsprung Disease Type 4c
|
|
Waardenburg Syndrome With Hirschsprung Disease, Type 4c
|
Waardenburg Syndrome, Type Ivc
|
|
Waardenburg Syndrome 4c
|
Hirschsprung Disease With Pigmentary Anomaly
|
|
Shah-Waardenburg Syndrome
|
Waardenburg-Shah Syndrome
|
|
Waardenburg Syndrome, Type 4a
|
|
|
| Auditory System Disease |
|
Ear Diseases
|
Ear And Mastoid Disease
|
|
|
| Deafness, Autosomal Dominant 22 |
|
DFNA22
|
Deafness, Autosomal Dominant 22, With Hypertrophic Cardiomyopathy
|
|
Autosomal Dominant Nonsyndromic Deafness 22
|
Progressive Sensorineural Hearing Loss-Hypertrophic Cardiomyopathy Syndrome
|
|
Autosomal Dominant Deafness 22
|
Progressive Neurosensory Deafness-Hypertrophic Cardiomyopathy Syndrome
|
|
Progressive Neurosensory Hearing Loss-Hypertrophic Cardiomyopathy Syndrome
|
Progressive Sensorineural Deafness-Hypertrophic Cardiomyopathy Syndrome
|
|
DFNHCM
|
Deafness, Autosomal Dominant, 22
|
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 22
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 22
|
|
Deafness, Autosomal Dominant, Type 22
|
Deafness, Autosomal Dominant Nonsyndromic Sensorineural 22
|
|
|
| Deafness, Autosomal Dominant 64 |
|
DFNA64
|
Autosomal Dominant Nonsyndromic Deafness 64
|
|
Autosomal Dominant Deafness 64
|
Deafness, Autosomal Dominant, 64
|
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 64
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 64
|
|
Deafness, Autosomal Dominant, Type 64
|
|
|
| Benign Familial Neonatal Epilepsy |
|
Familial Neonatal Seizures
|
Bfns
|
|
Benign Familial Neonatal Convulsions
|
Benign Familial Neonatal Seizures
|
|
Epilepsy Benign Neonatal Familial
|
Familial Benign Neonatal Convulsions
|
|
Benign Neonatal Familial Convulsions
|
Familial Benign Neonatal Epilepsy
|
|
Epilepsy, Benign Neonatal, 2
|
Benign Familial Convulsion
|
|
|
| Deafness, Autosomal Dominant 4a |
|
Deafness, Autosomal Dominant 4
|
DFNA4A
|
|
Dfna4
|
Autosomal Dominant Nonsyndromic Deafness 4a
|
|
Autosomal Dominant Deafness 4a
|
Deafness, Autosomal Dominant, 4a
|
|
Deafness Autosomal Dominant 4
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 4
|
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 4
|
Deafness, Autosomal Dominant, Type 4a
|
|
|
| Autosomal Dominant Nonsyndromic Deafness |
|
Autosomal Dominant Deafness
|
|
|
| Peripheral Vertigo |
|
|
| Branchiootorenal Syndrome 1 |
|
Melnick-Fraser Syndrome
|
BOR1
|
|
Branchiootorenal Dysplasia
|
Branchiootorenal Syndrome 1, With Or Without Cataracts
|
|
Bor Syndrome 1
|
Branchiootorenal Dysplasia 1
|
|
Branchio-Oto-Renal Dysplasia 1
|
Branchio-Oto-Renal Syndrome Type 1
|
|
Branchiootorenal Syndrome, With/Without Cataract, Type 1
|
Branchio-Oto-Renal Syndrome
|
|
|
| Vestibular Disease |
|
Vestibular Diseases
|
Vertigo, Vestibular Disorder
|
|
Vestibular Disorder
|
Diseases Of Inner Ear
|
|
|
| Waardenburg Syndrome, Type 1 |
|
Waardenburg Syndrome Type 1
|
WS1
|
|
Waardenburg Syndrome Type I
|
Waardenburg Syndrome With Dystopia Canthorum
|
|
Waardenburg'S Syndrome Type 1
|
Waardenburg Syndrome 1
|
|
Waardenburg Syndrome, Type I
|
Waardenburg Syndrome
|
|
|
| Inner Ear Disease |
|
Labyrinthine Dysfunction
|
Diseases Of Inner Ear
|
|
Labyrinthine Disease
|
Abnormality Of The Inner Ear
|
|
Labyrinth Diseases
|
Labyrinthine Disorder
|
|
Nonfunctioning Labyrinth
|
Labyrinthine Loss Of Function
|
|
Labyrinthine Syndrome
|
Labyrinthine Disorder Nos
|
|
|
| Meniere Disease |
|
Meniere'S Disease
|
Otogenic Vertigo
|
|
Ménière Disease
|
Ménière'S Disease
|
|
Mnire'S Vertigo
|
Auditory Vertigo
|
|
Aural Vertigo
|
Meniere'S Syndrome
|
|
Ménière'S Vertigo
|
Primary Endolymphatic Hydrops
|
|
Menieres Disease
|
Vertigo, Aural
|
|
Labyrinth Hydrops
|
Labyrinthine Hydrops
|
|
Labyrinthine Vertigo
|
Ménière Syndrome
|
|
Ménière Vertigo
|
Idiopathic Endolymphatic Hydrops
|
|
|
| Deafness, Autosomal Recessive 1a |
|
DFNB1A
|
Deafness, Digenic, Gjb2/Gjb3
|
|
Autosomal Recessive Nonsyndromic Deafness 1a
|
Deafness, Digenic, Gjb2/Gjb6
|
|
Deafness, Digenic Gjb2/Gjb6
|
Autosomal Recessive Deafness 1a
|
|
Deafness, Autosomal Recessive, 1a
|
Deafness Digenic Gjb2/Gjb3
|
|
Deafness Digenic Gjb2/Gjb6
|
Deafness Neurosensory Autosomal Recessive 1
|
|
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 1
|
Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 1
|
|
Nsrd1
|
Deafness, Autosomal Recessive, Type 1a
|
|
|
| Neonatal Period Electroclinical Syndrome |
|
|
| Long Qt Syndrome 1 |
|
Romano-Ward Syndrome
|
LQT1
|
|
Ward-Romano Syndrome
|
Rws
|
|
Ventricular Fibrillation With Prolonged Qt Interval
|
Wrs
|
|
Long Qt Syndrome 1, Acquired, Susceptibility To
|
Long Qt Syndrome 1, Acquired
|
|
Romano-Ward Long Qt Syndrome
|
Long Qt Syndrome Type 1
|
|
Long Qt Syndrome-1
|
Acquired Susceptibility To Long Qt Syndrome 1
|
|
Qt Syndrome, Long, Type 1
|
|
|
| Autosomal Recessive Nonsyndromic Deafness |
|
Deafness, Autosomal Recessive, Nonsyndromic
|
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt Syndrome
|
|
|
| Usher Syndrome |
|
Deafness-Retinitis Pigmentosa Syndrome
|
Dystrophia Retinae Pigmentosa-Dysostosis Syndrome
|
|
Graefe-Usher Syndrome
|
Hallgren Syndrome
|
|
Usher'S Syndrome
|
Retinitis Pigmentosa-Deafness Syndrome
|
|
Retinitis Pigmentosa-Hearing Loss Syndrome
|
Ush
|
|
Usher Syndromes
|
|
|
| Usher Syndrome, Type I |
|
USH1
|
Usher Syndrome Type 1
|
|
Us1
|
Usher Syndrome, Type 1b
|
|
Usher Syndrome Type 1e
|
Retinitis Pigmentosa And Congenital Deafness
|
|
Usher Syndrome, Type Ie
|
USH1E
|
|
Usher Syndrome, Type 1e
|
Usher Syndrome, Type 1a
|
|
Usher Syndrome, Type Ib
|
Usher Syndrome Type 1b
|
|
Usher Syndrome Type Ie
|
Usher Syndrome Type I
|
|
Usher 1
|
Usher Syndrome, Type 1
|
|
Ush1a
|
Usher Syndrome, Type I, French Variety
|
|
Usher Syndrome, Type Ia
|
Usher Syndrome 1b
|
|
USH1B
|
Usher'S Syndrome Type 1b
|
|
Usher Syndrome Type Ib
|
Ushib
|
|
|
| Familial Atrial Fibrillation |
|
Atrial Fibrillation, Familial
|
Atfb
|
|
Atrial Fibrillation Autosomal Dominant
|
Autosomal Dominant Atrial Fibrillation
|
|
Auricular Fibrillation
|
Atrial Fibrillation
|
|
Atrial Fibrillation, Familial, 1
|
|
|
| Benign Epilepsy With Centrotemporal Spikes |
|
Rolandic Epilepsy
|
Benign Rolandic Epilepsy
|
|
Epilepsy, Rolandic
|
Bcects
|
|
Benign Childhood Epilepsy With Centrotemporal Spike
|
Sylvan Seizures
|
|
Becrs
|
Bects
|
|
Bre
|
Benign Epilepsy Of Childhood With Centrotemporal Spikes
|
|
Benign Familial Epilepsy Of Childhood With Rolandic Spikes
|
Centrotemporal Epilepsy
|
|
|
