Moyamoya disease

disorder

SNOMED 69116000CUI C0026654

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.

Spider veins

Very frequent (80-99%)HP:0001009

Abnormality of the cerebral blood vessels

Frequent (30-79%)HP:0100659

Dilated cerebral ventricle

Frequent (30-79%)HP:0002119

Low intelligence

Frequent (30-79%)HP:0001249

Seizures

Frequent (30-79%)HP:0001250

Related Conditions

Moyamoya disease with early onset achalasia(child)

Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome(child)

Secondary moyamoya disease(child)

Cerebrovascular disease(parent)

Encephalopathy(parent)

Quick Facts

SNOMED CT: 69116000
UMLS CUI: C0026654
Fully Specified Name: Moyamoya disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.