← Back to Conditions

Congenital ichthyosis of skin

disorder
SNOMED 13059002CUI C0020758

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.

Ichthyosiform abnormality of the skin
Always present (100%)HP:0008064
Congenital lamellar ichthyosis
Very frequent (80-99%)HP:0007479
Everted eyelid
Very frequent (80-99%)HP:0000656
Palmoplantar keratosis
Very frequent (80-99%)HP:0000972
Congenital ichthyosiform erythroderma
Frequent (30-79%)HP:0007431
Hair loss
Frequent (30-79%)HP:0001596
Decreased hair growth
Occasional (5-29%)HP:0008070
Dystrophic nails
Occasional (5-29%)HP:0008404
Flexion contractures
Occasional (5-29%)HP:0001371
Nail dysplasia
Occasional (5-29%)HP:0002164
Desquamation of skin soon after birth
HP:0007549
Eclabium of lower lip
HP:0000232
Erythroderma
HP:0001019
Parakeratosis
HP:0001036
Thickening of upper layer of skin
HP:0025092

Quick Facts

SNOMED CT
13059002
UMLS CUI
C0020758
Fully Specified Name
Congenital ichthyosis of skin (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
15
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.