Immunodeficiency, X-linked, with deficiency of 115,000 dalton surface glycoprotein

Preferred Label : Immunodeficiency, X-linked, with deficiency of 115,000 dalton surface glycoprotein;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Gpl115 deficiency;

Inheritance : X-linked;

Prefixed ID : 308220;

Details

Origin ID

308220;

UMLS CUI

C1839982;

Currated CISMeF NLP mapping
- immunodeficiency, X-Linked, with deficiency of 115,000 dalton surface glycoprotein [MeSH Supplementary Concept]
- immunodeficiency, X-Linked, with deficiency of 115,000 dalton surface glycoprotein [MeSH concept]
HPO term(s)
- Abnormality of T cell physiology [HPO term]
- Recurrent bacterial infections [HPO term]
- Recurrent protozoan infections [HPO term]
- Recurrent viral infections [HPO term]
- X-linked inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- immunodeficiency, X-Linked, with deficiency of 115,000 dalton surface glycoprotein [MeSH Supplementary Concept]
- immunodeficiency, X-Linked, with deficiency of 115,000 dalton surface glycoprotein [MeSH concept]

Keyword's position in hierarchy(ies) :

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