Familial angiolipomatosis

disorder

SNOMED 774066000CUI C1859784

Overview

Familial angiolipomatosis 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.

Cutaneous angiolipomas

HP:0006773

Related Conditions

Angiolipoma(parent)

Recessive hereditary disorder (autosomal)(parent)

Hereditary disorder of the integument(parent)

Familial neoplastic disease(parent)

Quick Facts

SNOMED CT: 774066000
UMLS CUI: C1859784
Fully Specified Name: Familial angiolipomatosis (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.