Congenital ichthyosis

Preferred Label : Congenital ichthyosis;

ICD-10 exclusion note : Refsum's disease (G60.1);

Rare : true;

Source : OMS;

Date de début : 01/01/1997;

Do not code with : true;

Details

Origin ID

Q80;

UMLS CUI

C0020758;

Automatic exact mappings (from CISMeF team)
- Congenital ichthyosiform erythroderma [HPO term]
- congenital ichthyosis of skin, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- Congenital ichthyosis [MedDRA LLT]
- Congenital ichthyosis [HPO term]
- Congenital ichthyosis of skin (disorder) [SNOMED CT concept]
- Hereditary ichthyosis [Vue CIM-11]
- Ichthyosis congenita [ICD-9 code]
- Ichthyosis congenital [MedDRA LLT]
- Ichthyosis inherited [MedDRA LLT]
- Inherited ichthyosis [ORDO Disease]
- congenital ichthyosis [Disease (Nov.)]
- inherited ichthyosis [Disease (Nov.)]
Excluded by
- Acquired ichthyosis [ICD-10 Sub-category]
- Other conditions of integument specific to newborn [ICD-10 category]
ICD-10 exclusion(s)
- Refsum's disease [ICD-10 Sub-category]
Metaterm(s)
- dermatology [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital ichthyosis [MedDRA LLT]
- Congenital ichthyosis of skin (disorder) [SNOMED CT concept]
- Ichthyosis congenita [MedDRA LLT]
- Ichthyosis congenita [ICD-9 code]
- Ichthyosis congenital [MedDRA LLT]
- Ichthyosis, congenital, autosomal recessive 1 [OMIM Phenotype]
- autosomal recessive congenital ichthyosis 1 [DO Concept]
- congenital ichthyosis [Disease (Nov.)]
- congenital ichthyosis of skin, nos [SNOMED Notion]
- ichthyosis congenita I [MeSH concept]

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