All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05577 DEDSSH developmental delay with short stature, dysmorphic features, and sparse hair (DEDSSH) 616901 AR - 1 DPH1 - autosomal recessive
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