Steatocystoma multiplex

disorder

SNOMED 109433009CUI C0259771

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Sebaceous adenoma

Very frequent (80-99%)HP:0009720

Steatocystoma multiplex

Very frequent (80-99%)HP:0012035

Kidney stones

Occasional (5-29%)HP:0000787

Natal tooth

Excluded (<1%)HP:0000695

Related Conditions

Steatocystoma multiplex with natal tooth syndrome(child)

Hereditary disorder of the integument(parent)

Autosomal dominant hereditary disorder(parent)

Sebaceous cyst of skin(parent)

Quick Facts

SNOMED CT: 109433009
UMLS CUI: C0259771
Fully Specified Name: Steatocystoma multiplex (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 4

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.