All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02412 SPCH speech-language disorder (SPCH) - - 19 19 FOXP2 - -
05569 SPCH1 speech-language disorder, type 1 (SPCH-1) 602081 AD 1 1 FOXP2 - autosomal dominant
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