Femur-fibula-ulna syndrome

disorder

SNOMED 1230098009CUI C1856790

Overview

Femur-fibula-ulna 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

Abnormality of the thighbone

Very frequent (80-99%)HP:0002823

Absent/underdeveloped radius

Very frequent (80-99%)HP:0006501

Humeral hypoplasia

Very frequent (80-99%)HP:0005792

Humeral radial synostosis

Very frequent (80-99%)HP:0003041

Micromelia

Very frequent (80-99%)HP:0002983

Partial syndactyly

Very frequent (80-99%)HP:0006101

Split hand

Very frequent (80-99%)HP:0001171

Abnormal fibula morphology

Frequent (30-79%)HP:0002991

Abnormality of the elbow

Frequent (30-79%)HP:0009811

Amelia involving the upper limbs

Frequent (30-79%)HP:0009812

Unequal size of arms

Frequent (30-79%)HP:0100560

Decreased body height

Occasional (5-29%)HP:0004322

Peromelia

Occasional (5-29%)HP:0009828

Related Conditions

Dysostosis(parent)

Longitudinal deficiency of limb(parent)

Genetic disease(parent)

Congenital dysplasia of limb(parent)

Abnormality of limb bone morphology(parent)

Quick Facts

SNOMED CT: 1230098009
UMLS CUI: C1856790
Fully Specified Name: Femur fibula ulna complex (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.