Overview
Oculopalatocerebral 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.
Bronchial asthma
Very frequent (80-99%)HP:0002099
Decreased size of eyeball
Very frequent (80-99%)HP:0000568
Aplasia/Hypoplasia of the nails
Frequent (30-79%)HP:0008386
Cataract
Frequent (30-79%)HP:0000518
Cleft of palate
Frequent (30-79%)HP:0000175
Decreased body height
Frequent (30-79%)HP:0004322
Decreased size of cranium
Frequent (30-79%)HP:0000252
Disproportionately small hands
Frequent (30-79%)HP:0200055
Frontal cortex degeneration
Frequent (30-79%)HP:0006913
Hypoplastic or absent corpus callosum
Frequent (30-79%)HP:0007370
Intrauterine growth retardation, IUGR
Frequent (30-79%)HP:0001511
Involuntary muscle stiffness, contraction, or spasm
Frequent (30-79%)HP:0001257
Leukocoria
Frequent (30-79%)HP:0000555
Loose-jointedness
Frequent (30-79%)HP:0001382
Macrotia
Frequent (30-79%)HP:0000400
Mental and motor retardation
Frequent (30-79%)HP:0001263
Mental-retardation
Frequent (30-79%)HP:0001249
Narrow, high-arched roof of mouth
Frequent (30-79%)HP:0002705
Persistent hyperplasia of primary vitreous
Frequent (30-79%)HP:0007968
Small feet
Frequent (30-79%)HP:0001773
Thickened helices
Frequent (30-79%)HP:0000391
Generalised brain degeneration
Occasional (5-29%)HP:0002283
Glaucoma
Occasional (5-29%)HP:0000501
Retinal detachment
Occasional (5-29%)HP:0000541
Related Conditions
Quick Facts
- SNOMED CT
- 722055008
- UMLS CUI
- C1850338
- Fully Specified Name
- Oculopalatocerebral syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 24
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.