Lamellar ichthyosis

Preferred Label : Lamellar ichthyosis;

ICD-11 definition : Lamellar ichthyosis (LI) is a keratinization disorder characterized by the presence of large scales all over the body without significant erythroderma.;

ICD-11 synonym : Collodion baby;

ICD-11 inclusion : congenital lamellar ichthyosis; Collodion baby;

Details

Origin ID

600146417;

UMLS CUI

C0079154;

Automatic exact mappings (from CISMeF team)
- Collodion baby [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Lamellar Ichthyosis [NCIt concept]
- Lamellar ichthyosis [ORDO Disease]
- Lamellar ichthyosis [MedDRA LLT]
- Lamellar ichthyosis [ICD-10 Sub-category]
- Lamellar ichthyosis [ICD-10 Sub-category (who)]
- Lamellar ichthyosis (disorder) [SNOMED CT concept]
- Lamellar ichtyosis [PASCAL descriptor]
- ichthyosis, lamellar [MeSH concept]
- ichthyosis, lamellar [MeSH Descriptor]
- lamellar ichthyosis [Disease (Nov.)]
See also inter- (CISMeF)
- Collodion baby [PASCAL descriptor]
- Congenital ichthyosis [HPO term]
- Congenital ichthyosis [MedDRA LLT]
- Congenital ichthyosis of skin (disorder) [SNOMED CT concept]
- Ichthyosis congenita [ICD-9 code]
- Ichthyosis congenital [MedDRA LLT]
- autosomal recessive congenital ichthyosis [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Collodion baby [MedDRA Preferred Term]
- Congenital non bullous ichthyosiform erythroderma (disorder) [SNOMED CT concept]
- Congenital non-bullous ichthyosiform erythroderma [ORDO Disease]
- Congenital nonbullous ichthyosiform erythroderma [HPO term]
- Lamellar Ichthyosis [NCIt concept]
- Lamellar ichthyosis [ICD-10 Sub-category]
- Lamellar ichthyosis [MedDRA LLT]
- Lamellar ichthyosis [ORDO Disease]
- Lamellar ichthyosis (disorder) [SNOMED CT concept]
- Lamellar ichtyosis [PASCAL descriptor]
- autosomal recessive congenital ichthyosis [DO Concept]
- ichthyosis, lamellar [MeSH Descriptor]
- ichthyosis, lamellar [MeSH concept]
- lamellar ichthyosis [Disease (Nov.)]
Validated automatic mappings to BTNT
- Ichthyosis, congenital, autosomal recessive 1 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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