All diseases

OMIM ID
169100
OMIM term:
CHAR SYNDROME
Alternative terms:
CHAR
PATENT DUCTUS ARTERIOSUS WITH FACIAL DYSMORPHISM AND ABNORMAL FIFTH DIGITS
(∗) Location:
6p12.3  
(†) Associated OMIM genes:
TFAP2B  
(‡) Associated MGI genes:
Tfap2b  

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