| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) | Parent Node:
Blindness (D001766) | Parent Node:
Deafness (D003638) | ..Starting node
.. Deaf-Blind Disorders (D054062)
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Child Nodes:
| | ........Arts syndrome (C535388) | | ........Mohr-Tranebjaerg syndrome (C535808) | ........Usher Syndromes (D052245)  19 | | ........Weinstein Kliman Scully syndrome (C536688) | | ........Wittwer syndrome (C536737) | | ........Wolfram Syndrome (D014929) 1 |
Sister Nodes: | ..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)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 2977 |
| Name: | Deaf-Blind Disorders |
| Definition: | The absence of both hearing and vision. |
| Alternative IDs: | |
| ParentIDs: | MESH:D000015|MESH:D001766|MESH:D003638 |
| TreeNumbers: | C09.218.458.341.186.500 |C10.597.751.418.341.186.500 |C10.597.751.941.162.625 |C11.966.075.375 |C16.131.077.299 |C23.888.592.763.393.341.186.500 |C23.888.592.763.941.162.625 |
| Synonyms: | Blind-Deaf Disorder |Blind Deaf Disorders |Blind-Deaf Disorders |Blindness Deafness |Blindness-Deafness |Deaf-Blind Disorder |Deaf-Blind Disorder, Prelingual |Deaf Blind Disorders |Deaf-Blind Disorders, Prelingual |Deaf-Blindness Disorder |Deaf Blindness Disorders |
| Slim Mappings: | Congenital abnormality|Ear-nose-throat disease|Eye disease|Nervous system disease|Signs and symptoms |
| Reference: |
MedGen: D054062
MeSH: D054062
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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