- OMIM ID
-
182210
- OMIM term:
- SHPRINTZEN OMPHALOCELE SYNDROME
- Alternative terms:
-
OMPHALOCELE WITH HYPOPLASIA OF PHARYNX AND LARYNX, LEARNING DISABILITY, DYSMORPHIC FACIES, AND SCOLIOSIS
PHARYNX AND LARYNX HYPOPLASIA WITH OMPHALOCELE
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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