Indolent systemic mastocytosis

disorder

SNOMED 70910003CUI C0272203

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.

Abnormality of mastocytes

Very frequent (80-99%)HP:0100494

Abnormality of skin morphology

Very frequent (80-99%)HP:0011121

Bone marrow disease

Very frequent (80-99%)HP:0005561

Increased proportion of CD25+ mast cells

Very frequent (80-99%)HP:0031408

Mastocytosis

Very frequent (80-99%)HP:0100495

Abdominal cramps

Frequent (30-79%)HP:0032155

Allergy

Frequent (30-79%)HP:0012393

Darier's sign

Frequent (30-79%)HP:0025081

Elevated total serum tryptase

Frequent (30-79%)HP:0031901

Flushing

Frequent (30-79%)HP:0031284

Generalized abnormality of skin

Frequent (30-79%)HP:0011354

Hives

Frequent (30-79%)HP:0001025

Maculopapular exanthema

Frequent (30-79%)HP:0040186

Osteoporosis

Frequent (30-79%)HP:0000939

Skin itching

Frequent (30-79%)HP:0000989

Skin rash

Frequent (30-79%)HP:0000988

Anaphylactic reaction

Occasional (5-29%)HP:0100845

Enlarged liver

Very rare (1-4%)HP:0002240

Large spleen

Very rare (1-4%)HP:0001744

Lymph node hyperplasia

Very rare (1-4%)HP:0002716

Related Conditions

Systemic mast cell disease(parent)

Hematologic neoplasm of uncertain behavior(parent)

Quick Facts

SNOMED CT: 70910003
UMLS CUI: C0272203
Fully Specified Name: Indolent systemic mastocytosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 20

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.