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Congenital ichthyosis type 4

disorder
SNOMED 763401009CUI C1837610

Overview

Congenital ichthyosis type 4 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.

Caseous vernix-like desquamation
Always present (100%)HP:0025724
Epidermal hyperplasia
Always present (100%)HP:0025092
Erythroderma
Always present (100%)HP:0001019
Generalized ichthyosis
Always present (100%)HP:0007503
Hydramnios
Always present (100%)HP:0001561
Hyperkeratosis follicularis
Always present (100%)HP:0007502
Neonatal asphyxia
Always present (100%)HP:0012768
Skin itching
Always present (100%)HP:0000989
Desquamation of skin soon after birth
Very frequent (80-99%)HP:0007549
Eosinophilia
Very frequent (80-99%)HP:0001880
Ichthyosiform abnormality of the skin
Very frequent (80-99%)HP:0008064
Premature birth
Very frequent (80-99%)HP:0001622
Respiratory distress, neonatal
Very frequent (80-99%)HP:0002643
Baldness
Occasional (5-29%)HP:0002293
Nasal allergies
Occasional (5-29%)HP:0003193
Reaction to food allergens
Occasional (5-29%)HP:0500093
Reactive airway disease
Occasional (5-29%)HP:0002099
Dermatographic urticaria
HP:0011971
Patchy darkened skin
HP:0000953

Quick Facts

SNOMED CT
763401009
UMLS CUI
C1837610
Fully Specified Name
Ichthyosis prematurity syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
19
Clinical Trials
1
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.