All diseases

OMIM ID
194190
OMIM term:
WOLF-HIRSCHHORN SYNDROME; WHS
Alternative terms:
CHROMOSOME 4p16.3 DELETION SYNDROME
PITT-ROGERS-DANKS SYNDROME; PRDS
PITT SYNDROME
(∗) Location:
4p16.3  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Fgfrl1   Whsc1  

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