Ichthyosis - CISMeF

Preferred Label : Ichthyosis;

NCIt definition : A group of inherited or acquired skin disorders characterized by a dry, thickened, and scaly skin. The skin changes range from mild to severe.;

Details

Origin ID

C84776;

UMLS CUI

C0020757;

Automatic exact mappings (from CISMeF team)
- Congenital ichthyosis of skin (disorder) [SNOMED CT concept]
- congenital ichthyosis of skin, nos [SNOMED Notion]
- skin disease other [ICPC-2 Rubric]
Has associated anatomic sites
- Integumentary System [NCIt concept]
Manual BTNT mappings - CISMeF
- Congenital ichthyosis of skin (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ICHTHYOSIS [WHO-ART Included Term]
- Ichthyoses [MedDRA High Level Term]
- Ichthyosis [MedDRA Preferred Term]
- Ichthyosis [ORDO Disease]
- Ichthyosis [HPO term]
- Ichthyosis [HPO term]
- Ichthyosis [PASCAL descriptor]
- Ichthyosis (disorder) [SNOMED CT concept]
- Skin change ichthyosiform [MedDRA LLT]
- ichthyosis [DO Concept]
- ichthyosis [Disease (Nov.)]
- ichthyosis [MeSH Descriptor]
- ichthyosis [MeSH concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
disease_has_finding
- Cutaneous Involvement [NCIt concept]
disease_has_primary_anatomic_site
- Skin [NCIt concept]

Keyword's position in hierarchy(ies) :

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