Christianson Fourie syndrome

disorder

SNOMED 771239007CUI C1832411

Overview

Christianson Fourie syndrome 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.

Abnormal nail morphology

Very frequent (80-99%)HP:0001597

Abnormality of the hair shaft

Very frequent (80-99%)HP:0001595

Dystrophic nails

Very frequent (80-99%)HP:0008404

Loss of eyebrows

Very frequent (80-99%)HP:0002223

Onychogryphosis of toenails

Very frequent (80-99%)HP:0008401

Thin eyelashes

Very frequent (80-99%)HP:0000653

Thinning scalp hair

Very frequent (80-99%)HP:0002209

Decreased sexual hair

Frequent (30-79%)HP:0002225

Sparse axillary and pubic hair

Frequent (30-79%)HP:0002215

Cardiac arrhythmias

Occasional (5-29%)HP:0011675

Related Conditions

Hereditary disorder of the integument(parent)

Autosomal dominant hereditary disorder(parent)

Ectodermal dysplasia with hair-nail defect(parent)

Genetic disorder of nail(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 771239007
UMLS CUI: C1832411
Fully Specified Name: Hidrotic ectodermal dysplasia Christianson Fourie type (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.