Hereditary ichthyosis

Preferred Label : Hereditary ichthyosis;

ICD-11 definition : A range of disorders of markedly differing severities resulting from genetically determined defects in epidermal keratinization.;

ICD-11 synonym : Congenital ichthyosis;

Details

Origin ID

923829051;

Automatic exact mappings (from CISMeF team)
- Congenital ichthyosiform erythroderma [HPO term]
- congenital ichthyosis of skin, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- Congenital ichthyosis [ICD-10 category]
- Congenital ichthyosis [MedDRA LLT]
- Congenital ichthyosis [HPO term]
- Congenital ichthyosis of skin (disorder) [SNOMED CT concept]
- 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.)]
See also inter- (CISMeF)
- Ichthyosis, congenital, autosomal recessive 1 [OMIM Phenotype]
- Lamellar ichthyosis (disorder) [SNOMED CT concept]
- ichthyosis, lamellar [MeSH Descriptor]
Validated automatic mappings to BTNT
- autosomal recessive congenital ichthyosis 1 [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients