All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
07193 DFNB124 deafness, autosomal recessive, type 124 620794 AR - - PKHD1L1 - -
05086 HL hearing loss (HL) - - 1300 1187 C10orf90, FAM179A, GRAP, MPZL2, PDZD7, PKHD1L1, USP48 - -
04222 PKD kidney disease, polycystic (PKD) - - 1396 1292 GANAB, PKD1, PKD2, PKHD1 - -
02022 PKD4 kidney, polycystic, disease, type 4, with/without hepatic disease (PKD4) 263200 AR 8 7 PKHD1 - -
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