Cleft palate with stapes fixation and oligodontia syndrome

disorder

SNOMED 719468005CUI C4304738

Overview

Cleft palate with stapes fixation and oligodontia 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.

Abnormality of the ankle

Very frequent (80-99%)HP:0003028

Atretic auditory canal

Very frequent (80-99%)HP:0000413

Bilateral conductive hearing loss

Very frequent (80-99%)HP:0008513

Cleft of palate

Very frequent (80-99%)HP:0000175

Decreased number of baby teeth

Very frequent (80-99%)HP:0012225

Increased intercanthal distance

Very frequent (80-99%)HP:0000506

Tarsal bone synostosis

Very frequent (80-99%)HP:0008368

Abnormality of the wrist

Frequent (30-79%)HP:0003019

Fused wrist bones

Frequent (30-79%)HP:0009702

Related Conditions

Congenital fusion of ossicles of ear(parent)

Multiple system malformation syndrome(parent)

Recessive hereditary disorder (autosomal)(parent)

Auditory system hereditary disorder(parent)

Cleft of soft palate(parent)

Developmental absence of tooth(parent)

Oligodontia(parent)

Quick Facts

SNOMED CT: 719468005
UMLS CUI: C4304738
Fully Specified Name: Cleft palate with stapes fixation and oligodontia syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.