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
00248 MRXST mental retardation, X-linked syndromic, Turner type (MRXST) 300706 XL 2 2 HUWE1 - -
06874 MRXST Mental retardation, X-linked syndromic, Turner type 309590 XL 2 2 HUWE1 - -
00019 Xp11.22 microduplication microduplication syndrome, Xp11.22 (MRX17;MRX31) 300705 - - - HUWE1 - -
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