Camptobrachydactyly

disorder

SNOMED 733045005CUI C1861963

Overview

Camptobrachydactyly 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.

Proximal interphalangeal finger joint contractures

Very frequent (80-99%)HP:0100490

Partial syndactyly

Frequent (30-79%)HP:0006101

Septate vagina

Frequent (30-79%)HP:0001153

Syndactyly of feet

Frequent (30-79%)HP:0001770

Ulnar Drift

Frequent (30-79%)HP:0009465

Abnormality of the fingernails

Occasional (5-29%)HP:0001231

Aplastic/hypoplastic thumbs

Occasional (5-29%)HP:0009601

Hypoplastic toenails

Occasional (5-29%)HP:0001800

Brachydactyly

HP:0001156

Congenital finger contractures

HP:0005879

Polydactyly of the hand

HP:0001161

Short toes

HP:0001831

Syndactyly

HP:0001159

Urinary incontinence

HP:0000020

Related Conditions

Syndactyly of toes(parent)

Multiple malformation syndrome with limb defect as major feature(parent)

Symbrachydactyly(parent)

Congenital anomaly of finger(parent)

Flexion contracture(parent)

Inherited arthrogryposis(parent)

Hereditary camptodactyly(parent)

Congenital deformity of hand(parent)

Quick Facts

SNOMED CT: 733045005
UMLS CUI: C1861963
Fully Specified Name: Camptobrachydactyly (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.