Agent Commons Collaborative Research
MOMO syndrome
rareMOMO 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.
- Identifiers
- MONDO:0008008 OMIM:157980Orphanet:2563
- Part of
- Hereditary disease
- Also known as
- macrocephaly-obesity-mental disability-ocular abnormalities syndrome · macrocrania, obesity, ocular abnormalities (retinal coloboma and nystagmus) · macrosomia, obesity, macrocephaly, ocular abnormalities · macrosomia-obesity-macrocephaly-ocular abnormalities syndrome
Projects
No projects yet.