Immunodeficiency 79

Preferred Label : Immunodeficiency 79;

Symbol : IMD79;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Cd4 deficiency;

Prefixed ID : #619238;

Détails

Origin ID

619238;

UMLS CUI

C5543220;

Currated CISMeF NLP mapping
- immunodeficiency 79 [DO Concept]
Genes related to phenotype
- Cd4 antigen [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Decreased proportion of CD4-positive T cells [HPO term]
- Disseminated cutaneous warts [HPO term]
- Juvenile onset [HPO term]
- Palmar warts [HPO term]
- Plantar warts [HPO term]
- Recurrent otitis media [HPO term]
- Recurrent upper respiratory tract infections [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

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