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Macular cutaneous amyloidosis

disorder
SNOMED 111032003CUI C0546393

Overview

Macular cutaneous amyloidosis 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.

Diarrhea
Frequent (30-79%)HP:0002014
Leukopenia
Frequent (30-79%)HP:0001882
Low platelet count
Frequent (30-79%)HP:0001873
Malaise
Frequent (30-79%)HP:0033834
Positive gastric CMV intranuclear inclusions
Frequent (30-79%)HP:6001005
Tiredness
Frequent (30-79%)HP:0012378
Upset stomach
Frequent (30-79%)HP:0002027
Viral hepatitis
Frequent (30-79%)HP:0006562
Cytomegalovirus colitis
Occasional (5-29%)HP:0033431
Hepatic failure
Occasional (5-29%)HP:0001399
Inflammation of spinal cord
Occasional (5-29%)HP:0012486
Interstitial pneumonitis
Occasional (5-29%)HP:0006515
Viral encephalitis
Occasional (5-29%)HP:0033993
Retinitis
Very rare (1-4%)HP:0032118

Quick Facts

SNOMED CT
111032003
UMLS CUI
C0546393
Fully Specified Name
Macular cutaneous amyloidosis (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
14
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.