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
07056 KURIS Kury-Isidor syndrome 619762 AD 1 1 BAP1 - -
00381 RD dystrophy, retinal (RD) - - 277 210 C19orf44, UBAP1L - -
06829 SPG80 Spastic paraplegia 80, autosomal dominant 618418 AD - - UBAP1 - -
03606 TPDS tumor predisposition syndrome (TPDS) 614327 AD - - BAP1 - -
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