All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03170 DFNA2B deafness, autosomal dominant, type 2b (DFNA-2B) 612644 AD - - GJB3 - -
01745 DFNB1A deafness, autosomal recessive, type 1A (DFNB-1A, incl. di-genic) 220290 AR;DD 6 7 GJB2, GJB3, GJB6 - -
01324 EKVP1 erythrokeratodermia variabilis et progressiva, type 1 133200 AD;AR 18 18 GJA1, GJB3, GJB4 - -
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