Arthrogryposis hyperkeratosis syndrome lethal form

disorder

SNOMED 726620005CUI C1859710

Overview

Arthrogryposis hyperkeratosis syndrome lethal form 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.

Arthrogryposis multiplex

HP:0002804

Related Conditions

Congenital anomaly of skin(parent)

Skin lesion(parent)

Keratoderma(parent)

Arthrogryposis multiplex congenita(parent)

Quick Facts

SNOMED CT: 726620005
UMLS CUI: C1859710
Fully Specified Name: Arthrogryposis hyperkeratosis syndrome lethal form (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 1

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.