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MOMO syndrome

Disease Summary
Associated Targets (0)

Explore Associated Targets
Mondo Description MOMO syndrome is a very rare genetic overgrowth/obesity syndrome characterized by macrocephaly, obesity, mental (intellectual) disability and ocular abnormalities. Other frequent clinical signs include macrosomia, downslanting palpebral fissures, hypertelorism, broad nasal root, high and broad forehead and delay in bone maturation, in association with normal thyroid function and karyotype.
Mondo Term and Equivalent IDs
MONDO:0008008:  MOMO syndrome
GARD:0000178: 
MESH:C535812: 
Orphanet:2563: 
SCTID:724137002: 
UMLS:C1834759: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found