Hereditary progressive mucinous histiocytosis

disorder

SNOMED 771300001CUI C4749819

Overview

Hereditary progressive mucinous histiocytosis 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.

Erythematous macule

Very frequent (80-99%)HP:0025475

Erythematous papule

Very frequent (80-99%)HP:0030350

Mucinous histiocytosis

Very frequent (80-99%)HP:0040138

Skin itching

Occasional (5-29%)HP:0000989

Related Conditions

Chronic skin disease(parent)

Hereditary disorder of the integument(parent)

Non-Langerhans cell histiocytic dermatosis(parent)

Autosomal dominant hereditary disorder(parent)

Chronic histiocytosis(parent)

Quick Facts

SNOMED CT: 771300001
UMLS CUI: C4749819
Fully Specified Name: Hereditary progressive mucinous histiocytosis (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.