Microcephalus cleft palate syndrome

disorder

SNOMED 719394002CUI C2930954

Overview

Microcephalus cleft palate 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.

Cleft of palate

Very frequent (80-99%)HP:0000175

Decreased size of cranium

Very frequent (80-99%)HP:0000252

Submucous cleft hard palate

Very frequent (80-99%)HP:0000176

Uvula bifida

Very frequent (80-99%)HP:0000193

Abnormality of RPE

Occasional (5-29%)HP:0007703

Hypertrophy of mandible

Occasional (5-29%)HP:0000303

Hypoplastic mandible condyle

Occasional (5-29%)HP:0000347

Low intelligence

Occasional (5-29%)HP:0001249

Mental and motor retardation

Occasional (5-29%)HP:0001263

Proximal interphalangeal finger joint contractures

Occasional (5-29%)HP:0100490

Retrognathia

Occasional (5-29%)HP:0000278

Specific learning disability

Occasional (5-29%)HP:0001328

Related Conditions

Multiple malformation syndrome with facial defects as major feature(parent)

Cleft palate(parent)

Developmental hereditary disorder(parent)

Congenital microcephalus(parent)

Quick Facts

SNOMED CT: 719394002
UMLS CUI: C2930954
Fully Specified Name: Microcephalus cleft palate syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.