Immune suppression

Preferred Label : Immune suppression;

Symbol : IS;

CISMeF acronym : ISCW; IS; ISSCW;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : ISCW; Streptococcal cell wall antigen, suppression of immune response to; ISSCW;

Inheritance : Autosomal dominant;

Prefixed ID : 146850;

Details

Origin ID

146850;

UMLS CUI

C1840264;

Automatic exact mappings (from CISMeF team)
- Am Ag [LOINC component]
- Infantile spasms [ICD-11 Subcategory]
- adrenal insufficiency [MeSH Descriptor]
- equipment and supplies [MeSH Descriptor]
- instrumentation [MeSH Qualifier]
Currated CISMeF NLP mapping
- immunosuppression [Disease (Nov.)]
False automatic mappings
- Americium [NCIt concept]
- Androgen Response Element [NCIt concept]
- Are [NCIt concept]
- Armenia [NCIt concept]
- Attometer [NCIt concept]
- BES [MeSH concept]
- BES [MeSH Supplementary Concept]
- Bachelor of Engineering [NCIt concept]
- Barrett Esophagus [NCIt concept]
- Belgium [NCIt concept]
- Benign exophthalmos syndrome [ORDO Disease]
- Beryllium [NCIt concept]
- DNA Insertion Elements [NCIt concept]
- Iceland [NCIt concept]
- United Arab Emirates [NCIt concept]
- WAS Gene [NCIt concept]
- Wiskott-Aldrich Syndrome Protein [NCIt concept]
- bes [Substance BNPC]
- is (tumor staging) [SNOMED CT concept]
HPO term(s)
- Abnormality of the immune system [HPO term]
- Autosomal dominant inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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