All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04284 - dysplasia, ectodermal, hidrotic (Christianson-Fourie type) 601375 - 2 1 GJB6 - -
03169 DFNA3B deafness, autosomal dominant, type 3b (DFNA-3B) 612643 AD 1 1 GJB6 - -
01745 DFNB1A deafness, autosomal recessive, type 1A (DFNB-1A, incl. di-genic) 220290 AR;DD 6 7 GJB2, GJB3, GJB6 - -
03171 DFNB1B deafness, autosomal recessive, type 1b (DFNB-1B) 612645 AR 8 8 GJB6 - -
01299 ECTD2 dysplasia, ectodermal, type 2 (ECTD-2, Clouston syndrome) 129500 AD 15 15 GJB6 - -
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