Immunodeficiency 88

Preferred Label : Immunodeficiency 88;

Symbol : IMD88;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Immunodeficiency 88, mycobacteriosis, autosomal recessive;

Prefixed ID : #619630;

Details

Origin ID

619630;

UMLS CUI

C5562026;

Genes related to phenotype
- T-box transcription factor 21 [OMIM gene]
HPO term(s)
- Asthma [HPO term]
- Autosomal recessive inheritance [HPO term]
- BCGosis [HPO term]
- Eosinophilia [HPO term]
- Infantile onset [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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