Brachydactyly type A4

disorder

SNOMED 715721005CUI C1862139

Overview

Brachydactyly type A4 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.

Shortening of all the middle bones of the toes

Very frequent (80-99%)HP:0006239

Decreased body height

Frequent (30-79%)HP:0004322

Foot, talipes equinovarus

Occasional (5-29%)HP:0001762

Aplasia of the middle phalanges of the toes

HP:0100387

Congenital talipes calcaneovalgus

HP:0005850

Short middle bone of index finger

HP:0009577

Talipes calcaneovalgus

HP:0001884

Type A brachydactyly

HP:0009370

Type A3 brachydactyly

HP:0004220

Related Conditions

Autosomal dominant hereditary disorder(parent)

Brachymesophalangia(parent)

Hereditary disorder of musculoskeletal system(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 715721005
UMLS CUI: C1862139
Fully Specified Name: Brachydactyly type A4 (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.