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Congenital hypertrichosis lanuginosa

disorder
SNOMED 403799003CUI C0235864

Overview

Congenital hypertrichosis lanuginosa 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.

Deafness
Very frequent (80-99%)HP:0000365
Delayed eruption of teeth
Very frequent (80-99%)HP:0000684
Dental problems
Very frequent (80-99%)HP:0000164
Generalized hirsutism
Very frequent (80-99%)HP:0002230
Thick eyebrow
Very frequent (80-99%)HP:0000574
Abnormal skin colour
Frequent (30-79%)HP:0001000
Gingival hyperplasia
Occasional (5-29%)HP:0000212
Double eyebrow
HP:0010730
Hypertrichosis universalis
HP:0004540

Quick Facts

SNOMED CT
403799003
UMLS CUI
C0235864
Fully Specified Name
Congenital hypertrichosis lanuginosa (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
9
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.