Robin sequence and oligodactyly syndrome

disorder

SNOMED 770681000CUI C4749398

Overview

Robin sequence and oligodactyly 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.

Abnormal morphology of ulna

Very frequent (80-99%)HP:0040071

Absent fingers

Very frequent (80-99%)HP:0009380

Decreased projection of lower jaw

Very frequent (80-99%)HP:0000347

Retraction of the tongue

Very frequent (80-99%)HP:0000162

Abnormal metacarpal morphology

Frequent (30-79%)HP:0005916

Cleft of palate

Frequent (30-79%)HP:0000175

Decreased transverse dimension of face

Frequent (30-79%)HP:0000275

Dental problems

Frequent (30-79%)HP:0000164

Permanent curving of the pinkie finger

Frequent (30-79%)HP:0004209

Abnormal vertebral bodies

Occasional (5-29%)HP:0003312

Related Conditions

Robin sequence(parent)

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

Adactyly(parent)

Quick Facts

SNOMED CT: 770681000
UMLS CUI: C4749398
Fully Specified Name: Robin sequence and oligodactyly syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.