Congenital generalised hypertrichosis

disorder

SNOMED 838368005CUI C5574955

Overview

Congenital generalised hypertrichosis is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

X-linked congenital generalized hypertrichosis(child)

FHEIG (facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth) syndrome(child)

Congenital hypertrichosis(parent)

Quick Facts

SNOMED CT: 838368005
UMLS CUI: C5574955
Fully Specified Name: Congenital generalized hypertrichosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.