ichthyosis vulgaris

Preferred Label : ichthyosis vulgaris;

MeSH definition : Most common form of ICHTHYOSIS characterized by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait.;

MeSH synonym : ichthyosis vulgaris, dominant; dominant ichthyosis vulgaris; ichthyosis simplex; ichthyosis simplices;

MeSH annotation : do not use /congen & do not coord with INFANT, NEWBORN, DISEASES;

Details

Origin ID

D016112;

UMLS CUI

C0079584;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Bullous ichthyosiform erythroderma (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Autosomal dominant ichthyosis vulgaris [ORDO Disease]
- Dominant congenital ichthyosiform erythroderma (disorder) [Inactive SNOMED CT concept]
- Ichthyosis Vulgaris [NCIt concept]
- Ichthyosis vulgaris [PASCAL descriptor]
- Ichthyosis vulgaris [ICD-10 Sub-category]
- Ichthyosis vulgaris [ICD-10 Sub-category (who)]
- Ichthyosis vulgaris [ICD-11 Sub-sub category]
- Ichthyosis vulgaris [MedDRA LLT]
- Ichthyosis vulgaris (disorder) [SNOMED CT concept]
- ichthyosis vulgaris [DO Concept]
- ichthyosis vulgaris [Disease (Nov.)]
DO Cross reference
- ichthyosis vulgaris [DO Concept]
Has phenotype(s) (HPO)
- Ichthyosis [HPO term]
Record concept(s)
- ichthyosis vulgaris [MeSH concept]
Related MeSH Supplementary Concept(s)
- osteosclerosis with ichthyosis and premature ovarian failure [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant ichthyosis vulgaris [ORDO Disease]
- Dominant congenital ichthyosiform erythroderma (disorder) [Inactive SNOMED CT concept]
- Ichthyosis Vulgaris [NCIt concept]
- Ichthyosis vulgaris [MedDRA LLT]
- Ichthyosis vulgaris [OMIM Phenotype]
- Ichthyosis vulgaris [ICD-10 Sub-category]
- Ichthyosis vulgaris [ICD-10 Sub-category (who)]
- Ichthyosis vulgaris [PASCAL descriptor]
- Ichthyosis vulgaris [ICD-11 Sub-sub category]
- Ichthyosis vulgaris (disorder) [SNOMED CT concept]
- dominant congenital ichthyosiform erythroderma [SNOMED Notion]
- ichthyosis vulgaris [DO Concept]
- ichthyosis vulgaris [Disease (Nov.)]
Validated automatic mappings to BTNT
- Autosomal dominant ichthyosis vulgaris (disorder) [SNOMED CT concept]
- Ichthyosis vulgaris [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

Main resources

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