Autoimmune disease

Preferred Label : Autoimmune disease;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant gene epistatic to other secondary genes conferring specificity to the autoimmune phenotype;

Prefixed ID : #109100;

Détails

Origin ID

109100;

UMLS CUI

C0004364;

Automatic exact mappings (from CISMeF team)
- Autoimmune disease [PASCAL descriptor]
- autoimmune disease [DO Concept]
- autoimmune disease [OBI concept]
- autoimmune disease [COVID-19 Thesaurus concept]
- autoimmune disease [Blood Transfusion thesaurus concept]
DO Cross reference
- autoimmune disease [DO Concept]
HPO term(s)
- Autoimmune antibody positivity [HPO term]
- Autoimmunity [HPO term]
- Autosomal dominant inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- AUTOIMMUNE DISORDER NOS [WHO-ART Included Term]
- Autoimmune Disease [NCIt concept]
- Autoimmune disease [LOINC component]
- Autoimmune disease (disorder) [SNOMED CT concept]
- Autoimmune disease flare up [MedDRA LLT]
- Autoimmune diseases [LOINC component]
- Autoimmune disorder [MedDRA Preferred Term]
- Autoimmune disorder NOS [MedDRA LLT]
- Autoimmune disorders [MedDRA High Level Group Term]
- Autoimmunity [HPO term]
- autoimmune disease [Radlex concept]
- autoimmune disease, nos [SNOMED Notion]
- autoimmune diseases [MedlinePlus Topic]
- autoimmune diseases [MeSH Descriptor]
- autoimmune diseases [MeSH concept]
- autoimmune disorder [Disease (Nov.)]

Position du mot-clé dans l'(les) arborescence(s) :

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