Bifid femur co-occurrent with monodactylous ectrodactyly

disorder

SNOMED 716006003CUI C1856789

Overview

Bifid femur co-occurrent with monodactylous ectrodactyly 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.

Aplasia/Hypoplasia of the tibia

Very frequent (80-99%)HP:0005772

Ectrodactyly

Very frequent (80-99%)HP:0100257

Hypoplasia or unilateral/bilateral absence of ulna

Frequent (30-79%)HP:0006495

Absent ossification/absent ulna

HP:0003982

Absent shinbone

HP:0009556

Foot monodactyly

HP:0200054

Hand monodactyly

HP:0004058

Split hand

HP:0001171

Split thighbone

HP:0010443

Related Conditions

Ectrodactyly(parent)

Hereditary disorder of musculoskeletal system(parent)

Congenital abnormal shape of femur(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 716006003
UMLS CUI: C1856789
Fully Specified Name: Bifid femur co-occurrent with monodactylous ectrodactyly (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.