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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Braddock-Carey Syndrome 1 
Braddock-Carey Syndrome 2  
Characterized by congenital thrombocytopenia, microcephaly, and facial dysmorphisms including Pierre-Robin sequence. Caused by homozygous mutation in the KIF15 gene on chromosome 3p21.

Synonyms
Exact Synonyms: BRDCS2
Primary IDs: OMIM:619981
Definition Sources: OMIM:619981

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