Immunodeficiency 86

Preferred Label : Immunodeficiency 86;

Symbol : IMD86;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Immunodeficiency 86, mycobacteriosis, autosomal recessive;

Prefixed ID : #619549;

Details

Origin ID

619549;

UMLS CUI

C5561995;

Genes related to phenotype
- Signal peptide peptidase-like 2a [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- BCGitis [HPO term]
- Decreased circulating IgG level [HPO term]
- Impaired oxidative burst [HPO term]
- Increased circulating IgM level [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients