All diseases

OMIM ID
119500
OMIM term:
POPLITEAL PTERYGIUM SYNDROME; PPS
Alternative terms:
CLEFT LIP/PALATE, PARAMEDIAN MUCOUS CYSTS OF THE LOWER LIP, POPLITEAL PTERYGIUM, DIGITAL AND GENITAL ANOMALIES
FACIOGENITOPOPLITEAL SYNDROME
(∗) Location:
1q32.2  
(†) Associated OMIM genes:
IRF6  
(‡) Associated MGI genes:
Irf6  

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