| Disease Browser
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Parent Node:
 Hearing Loss (D034381) |
..Starting node
.. Deafness (D003638)
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Child Nodes:
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| ........Albinism deafness syndrome (C537042) |
| ........ALPORT SYNDROME, X-LINKED (OMIM:301050) |
| ........Arthrogryposis multiplex with deafness, inguinal hernias, and early death (C535381) |
| ........Ayazi syndrome (C537793) |
| ........Branchiogenic-Deafness Syndrome (C563780) |
| ........Burn-Mckeown syndrome (C537411) |
| ........Cardioauditory syndrome of Sanchez Cascos (C535577) |
| ........Charcot-Marie-Tooth Disease, Demyelinating, Type 1e (C566136) |
| ........Corneal Degeneration, Ribbonlike, with Deafness (C565157) |
| ........Coxoauricular Syndrome (C565148) |
| ........Davenport Donlan syndrome (C535988) |
........Deaf-Blind Disorders (D054062)  26 |
| ........Deafness hyperuricemia neurologic ataxia (C535995) |
| ........Deafness with Labyrinthine Aplasia Microtia and Microdontia (LAMM) (C548011) |
| ........DEAFNESS, AUTOSOMAL DOMINANT 22;DFNA22 DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY, (OMIM:606346) |
| ........DEAFNESS, AUTOSOMAL DOMINANT 27 (OMIM:612431) |
| ........DEAFNESS, AUTOSOMAL DOMINANT 33 (OMIM:614211) |
| ........DEAFNESS, AUTOSOMAL DOMINANT 4A (OMIM:600652) |
| ........DEAFNESS, AUTOSOMAL DOMINANT 50 (OMIM:613074) |
| ........DEAFNESS, AUTOSOMAL DOMINANT 51 (OMIM:613558) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 18A (OMIM:602092) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 25 (OMIM:613285) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT (OMIM:609006) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT (OMIM:600791) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 45 (OMIM:612433) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 74 (OMIM:613718) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 83 (OMIM:613685) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 84A (OMIM:613391) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 85 (OMIM:613392) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 89 (OMIM:613916) |
| ........DEAFNESS, AUTOSOMAL RECESSIVE 91 (OMIM:613453) |
| ........Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities (C567467) |
| ........Deafness, congenital onychodystrophy, recessive form (C538204) |
| ........Deafness, Congenital, and Familial Myoclonic Epilepsy (C565649) |
| ........Deafness, Congenital, and Onychodystrophy, Autosomal Dominant (C567274) |
| ........Deafness, Congenital, with Vitiligo and Achalasia (C565642) |
| ........DEAFNESS, NONSYNDROMIC, MODIFIER 1 (OMIM:605429) |
| ........DEAFNESS, Y-LINKED 1 (OMIM:400043) |
| ........Dementia, familial Danish (C538209) |
| ........Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation (C566408) |
| ........Emphysema, Congenital, With Deafness, Penoscrotal Web, And Mental Retardation (C566519) |
| ........Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness (C565585) |
| ........Fine-Lubinsky syndrome (C537933) |
| ........Fountain syndrome (C537270) |
| ........Herrmann syndrome (C538113) |
| ........Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness (C565518) |
| ........Hyperlipoproteinemia, Type II, and Deafness (C564170) |
| ........HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS (OMIM:614187) |
| ........Ichthyosiform erythroderma, corneal involvement, deafness (C537363) |
| ........Johnson neuroectodermal syndrome (C535882) |
| ........Jones syndrome (C535886) |
| ........Keratitis, Ichthyosis, and Deafness (KID) Syndrome (C536168) |
| ........Konigsmark Knox Hussels syndrome (C537214) |
| ........Lynch Lee Murday syndrome (C537713) |
| ........Mental retardation-hypotonic facies syndrome, x-linked, 1 (C537457) |
| ........Meyenburg-Altherr-Uehlinger syndrome (C537574) |
| ........Microcephaly deafness syndrome (C537326) |
| ........MUCKLE-WELLS SYNDROME (OMIM:191900) |
| ........MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500) |
| ........Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders (C565786) |
| ........Myoclonus, Cerebellar Ataxia, and Deafness (C563549) |
| ........Nasodigitoacoustic syndrome (C538337) |
| ........Nathalie syndrome (C538342) |
| ........Nephrosis deafness urinary tract digital malformation (C536402) |
| ........Noninsulin-dependent diabetes mellitus with deafness (C536246) |
| ........Nonsyndromic Deafness (C580334) |
| ........Opticocochleodentate Degeneration (C563002) |
| ........PERRAULT SYNDROME 3 (OMIM:614129) |
| ........Ramos Arroyo Clark syndrome (C535286) |
| ........Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness (C567595) |
| ........Richards-Rundle syndrome (C535674) |
| ........Schimke X-linked mental retardation syndrome (C536630) |
| ........Schlegelberger Grote syndrome (C536635) |
| ........Secretory Diarrhea, Myopathy, and Deafness (C564382) |
| ........Spastic paraplegia 24 (C536860) |
| ........Temtamy preaxial brachydactyly syndrome (C536958) |
| ........Tibia, Absence of, with Congenital Deafness (C564764) |
| ........Tietz syndrome (C536919) |
| ........Wells Jankovic syndrome (C536692) |
| ........Wright Dyck syndrome (C536749) |
| ........X-linked mental retardation Gustavson type (C536759) |
| ........Yemenite deaf-blind hypopigmentation syndrome (C536771) |
Sister Nodes: |
..Abidi X-linked mental retardation syndrome (C535556)
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..Behr syndrome (C537669)
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..Branchial arch syndrome X-linked (C537102)
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..CATSHL syndrome (C537975)
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..Chromosome 6pter-P24 Deletion Syndrome (C567239)
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..Deafness (D003638) 108
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..Deafness with Anhidrotic Ectodermal Dysplasia (C565119)
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..Deafness, Autosomal Dominant, Due To Mutation In Myo1a (C567266)
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..Deafness, Autosomal Recessive 36, Without Vestibular Involvement (C567219)
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..Deafness, Congenital Heart Defects, and Posterior Embryotoxon (C566604)
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..Deafness, Unilateral, With Delayed Endolymphatic Hydrops (C567420)
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..Deafness-Craniofacial Syndrome (C565118)
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..Hearing Loss, Bilateral (D006312) 5
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..HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO (OMIM:613290)
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..Hearing Loss, Conductive (D006314) 21
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..Hearing Loss, Functional (D006315)
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..Hearing Loss, High-Frequency (D006316)
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..Hearing Loss, Mixed Conductive-Sensorineural (D046089) 3
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..Hearing Loss, Sensorineural (D006319) 252
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..Hearing Loss, Sudden (D003639)
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..Hearing Loss, Unilateral (D046088) 1
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..Iris dysplasia hypertelorism deafness (C535537)
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..Lacrimoauriculodentodigital syndrome (C538132)
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..Microcephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance (C567849)
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..Microtia, Hearing Impairment, And Cleft Palate (C567359)
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..Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay (C567769)
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..Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant (C563497)
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..Reardon Wilson Cavanagh syndrome (C535295)
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..Spondylomegaepiphyseal Dysplasia With Upper Limb Mesomelia, Punctate Calcifications, And Deafness (C566507)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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