Immunodeficiency 77

Preferred Label : Immunodeficiency 77;

Symbol : IMD77;

Type : Phenotype, molecular basis known;

Prefixed ID : #619223;

Origin ID

619223;

UMLS CUI

C5543173;

Genes related to phenotype
- Macrophage expressed gene 1 [OMIM gene]
HPO term(s)
- Adult onset [HPO term]
- Autosomal dominant inheritance [HPO term]
- Bilateral sensorineural hearing impairment [HPO term]
- Bronchiectasis [HPO term]
- Cellulitis [HPO term]
- Chronic pulmonary obstruction [HPO term]
- Cutaneous abscess [HPO term]
- Gastroparesis [HPO term]
- Nontuberculous mycobacterial pulmonary infection [HPO term]
- Recurrent tonsillitis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]