MYD88 deficiency

Preferred Label : MYD88 deficiency;

MeSH note : mutation in MYD88;

MeSH synonym : MYD88D; pyogenic bacterial infections, recurrent, due to MYD88 deficiency; recurrent pyogenic bacterial infections due to MYD88 deficiency;

Details

Origin ID

C567379;

UMLS CUI

C2677092;

Currated CISMeF NLP mapping
- Bacterial susceptibility due to TLR signaling pathway deficiency [ORDO Disease]
- Immunodeficiency 68 [OMIM Phenotype]
MeSH term(s) associated for indexing
- Primary Immunodeficiency Diseases [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- MYD88 deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Bacterial susceptibility due to TLR signaling pathway deficiency [ORDO Disease]
- Immunodeficiency 68 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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