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
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
02259 PMD;HLD1 Pelizaeus-Merzbacher disease (PMD, hypomyelinative leukodystrophy (HLD-1)) 312080 XLR 77 77 PLP1 - X-linked recessive
02264 SPG2 paraplegia, spastic, type 2 (SPG-2) 312920 XLR - - PLP1 - X-linked recessive
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