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) - - 977 973 CDH23, CIB2, FAM65B, GIPC3, GRXCR1, HGF, MYO15A, MYO7A, OTOF, OTOG, PCDH15, RDX, S1PR2, SERPINB6, STRC, TMC1, USH1C - autosomal recessive
03299 DFNB25 deafness, autosomal recessive, type 25 (DFNB-25) 613285 AR 5 1 GRXCR1 - -
02850 HIVS virus, human immunodeficiency, susceptibility to 609423 - 1 1 CCL11, CCL2, CCL3, CCL3L1, CD209, CX3CR1, CXCL12, CXCR1, HLA-C, IFNG, IL10, IL4R, KIR3DL1, TLR3 - -
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