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
05400 DFNB deafness, autosomal recessive (DFNB) - - 955 951 CDH23, CIB2, FAM65B, GRXCR1, HGF, MYO15A, MYO7A, OTOF, OTOG, PCDH15, RDX, S1PR2, SERPINB6, STRC, TMC1, USH1C - autosomal recessive
03003 DFNB24 deafness, autosomal recessive, type 24 611022 AR 1 1 RDX - -
02120 MAHCC aciduria, methylmalonic, and homocystinuria, cblC type (MAHCC) 277400 AR 4 4 MMACHC, PRDX1 - -
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