Congenital ichthyosis with hypotrichosis syndrome

disorder

SNOMED 724277002CUI C4510566

Overview

Congenital ichthyosis with hypotrichosis 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.

Hypotrichosis

Very frequent (80-99%)HP:0008070

Ichthyosiform abnormality of the skin

Very frequent (80-99%)HP:0008064

Related Conditions

Congenital hypotrichia(parent)

Autosomal recessive ichthyosis(parent)

Quick Facts

SNOMED CT: 724277002
UMLS CUI: C4510566
Fully Specified Name: Congenital ichthyosis with hypotrichosis syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 2

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.