Brachydactyly type A6

disorder

SNOMED 715722003CUI C1862130

Overview

Brachydactyly type A6 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 backbone

HP:0000925

Bipartite calcaneus

HP:0008127

Decreased body height

HP:0004322

Decreased finger mobility

HP:0006135

Dysplastic distal radial epiphyses

HP:0005013

Fused wrist bones

HP:0009702

Hypoplastic/aplastic middle phalanx

HP:0009843

Mesomelia

HP:0003027

Phalangeal hypoplasia

HP:0009803

Radial deviation of finger

HP:0009466

Radial ray hypoplasia

HP:0002984

Short fibula

HP:0003038

Short skankbone

HP:0005736

Short toes

HP:0001831

Short ulna

HP:0003022

Tarsal bone synostosis

HP:0008368

Type A brachydactyly

HP:0009370

Wide fingers

HP:0001500

Wide toe

HP:0001837

Related Conditions

Autosomal dominant hereditary disorder(parent)

Brachymesophalangia(parent)

Hereditary disorder of musculoskeletal system(parent)

Developmental hereditary disorder(parent)

Mesomelic dysplasia(parent)

Quick Facts

SNOMED CT: 715722003
UMLS CUI: C1862130
Fully Specified Name: Brachydactyly type A6 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 19

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.