obsolete_MOMO syndrome true http://purl.obolibrary.org/obo/MONDO_0008008 Macrosomia-obesity-macrocephaly-ocular abnormalities syndrome 3.41.0 OMIM:157980 MOMO syndrome is a very rare genetic overgrowth/obesity syndrome (see this term) characterized by macrocephaly, obesity, mental (intellectual) disability and ocular abnormalities. Other frequent clinical signs include macrosomia, downslanting palpebral fissures, hypertelorism, broad nasal root, high broad forehead and delay in bone maturation in association with normal thyroid function and karyotype. Replaced with Mondo term. ICD10:Q87.3 UMLS:C1834759 Macrocephaly-obesity-mental disability-ocular abnormalities syndrome orphanet