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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/612644
http://purl.bioontology.org/ontology/OMIM/612644
|
|---|---|
| Preferred Name | DEAFNESS, AUTOSOMAL DOMINANT 2B |
| Synonyms |
DFNA2B
DEAFNESS, AUTOSOMAL DOMINANT, WITH OR WITHOUT PERIPHERAL NEUROPATHY
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
DFNA2B
DEAFNESS, AUTOSOMAL DOMINANT, WITH OR WITHOUT PERIPHERAL NEUROPATHY
|
|---|---|
| prefLabel | DEAFNESS, AUTOSOMAL DOMINANT 2B
|
| Gene Symbol |
EKVP1
CX31
GJB3
DFNA2B
|
| Scope Statement | Caused by mutation in the gap junction protein, beta-3 gene (GJB3, 603324.0004) [MOLECULAR BASIS]
|
| type | |
| Has manifestation | |
| tui | T047
|
| Gene Locus | 1p35.1
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 612644
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C2675236
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |