Overview
MOMO syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Obesity
Always present (100%)HP:0001513
Abnormal bone ossification
Frequent (30-79%)HP:0011849
Auditory sensitivity
Frequent (30-79%)HP:0025112
Bilateral crossbite
Frequent (30-79%)HP:0000689
Bilateral nanophthalmos
Frequent (30-79%)HP:0007633
Bowed femura
Frequent (30-79%)HP:0002980
Chorioretinal coloboma
Frequent (30-79%)HP:0000567
Cutis marmorata
Frequent (30-79%)HP:0000965
Decreased body height
Frequent (30-79%)HP:0004322
Delayed eruption of teeth
Frequent (30-79%)HP:0000684
Disproportionately large hands
Frequent (30-79%)HP:0001176
Down-slanting palpebral fissure
Frequent (30-79%)HP:0000494
Epilepsy
Frequent (30-79%)HP:0001250
Eyelid coloboma
Frequent (30-79%)HP:0000625
Fetal macrosomia
Frequent (30-79%)HP:0001520
Full lower lip
Frequent (30-79%)HP:0000179
Full upper lip
Frequent (30-79%)HP:0000215
General overgrowth
Frequent (30-79%)HP:0001548
High arched palate
Frequent (30-79%)HP:0000218
High forehead
Frequent (30-79%)HP:0000348
Increased distance between eyes
Frequent (30-79%)HP:0000316
Increased size of skull
Frequent (30-79%)HP:0000256
Increased width of the forehead
Frequent (30-79%)HP:0000337
Involuntary, rapid, rhythmic eye movements
Frequent (30-79%)HP:0000639
Long foot
Frequent (30-79%)HP:0001833
Nail overcurvature
Frequent (30-79%)HP:0001795
Nonprogressive mental retardation
Frequent (30-79%)HP:0001249
Palpebronasal fold
Frequent (30-79%)HP:0000286
Poorly folded helices
Frequent (30-79%)HP:0008577
Short and broad skull
Frequent (30-79%)HP:0000248
Related Conditions
Multiple malformation syndrome with early overgrowth(parent)
Recessive hereditary disorder (autosomal)(parent)
Congenital anomaly of visual system(parent)
Hereditary disorder of the visual system(parent)
Disorder of eye region(parent)
Developmental hereditary disorder(parent)
Congenital macrocephaly(parent)
Genetic obesity disorder(parent)
Genetic intellectual disability(parent)
Quick Facts
- SNOMED CT
- 724137002
- UMLS CUI
- C1834759
- Fully Specified Name
- Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.