Autosomal recessive aplasia cutis congenita of limb

disorder

SNOMED 723500009CUI C1838206

Overview

Autosomal recessive aplasia cutis congenita of limb 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.

Congenital absence of skin of limbs

HP:0007506

Congenital scars

HP:0001057

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Hereditary disorder of the integument(parent)

Aplasia cutis congenita of limb(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 723500009
UMLS CUI: C1838206
Fully Specified Name: Autosomal recessive aplasia cutis congenita of limb (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 2

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.