Erythroderma, lethal congenital

Preferred Label : Erythroderma, lethal congenital;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal recessive;

Prefixed ID : %227090;

Details

Origin ID

227090;

UMLS CUI

C1856898;

Currated CISMeF NLP mapping
- Congenital lethal erythroderma [ORDO Disease]
- Congenital lethal erythroderma (disorder) [SNOMED CT concept]
- Lethal congenital erythroderma [MeSH concept]
- lethal congenital erythroderma [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Congenital exfoliative erythroderma [HPO term]
- Death in infancy [HPO term]
- Failure to thrive [HPO term]
- Hypoalbuminemia [HPO term]
ORDO concept(s)
- Congenital lethal erythroderma [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital lethal erythroderma [ORDO Disease]
- Congenital lethal erythroderma (disorder) [SNOMED CT concept]
- Lethal congenital erythroderma [MeSH concept]
- lethal congenital erythroderma [MeSH Supplementary Concept]

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