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
01060 KFSDX keratosis follicularis spinulosa decalvans, X-linked (KFSDX) 308800 XLR 4 4 MBTPS2, SAT1 - -
04631 NLS2 Neu-Laxova syndrome, tyep 2 (NLS-2) 616038 AR 13 13 PSAT1 - -
03002 PSATD deficiency, phosphoserine aminotransferase (PSATD) 610992 AR 2 2 PSAT1 - -
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