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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Bartsocas-Papas Syndrome 1  
Bartsocas-Papas Syndrome 2  
A severe form of popliteal pterygium disorder characterized by cutaneous webbing across one or more joints, cleft lip and/or palate, syndactyly, and genital malformations. Caused by homozygous mutation in the CHUK gene on chromosome 10q24. (OMIM)
Familial Popliteal Pterygium Syndrome 

Synonyms
Exact Synonyms: BPS2 ;   popliteal pterygium syndrome, Bartsocas-Papas type 2
Primary IDs: OMIM:619339

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