ZFIN Human Disease: immunodeficiency 39

OBO ID: DOID:0111969

Term Name:	immunodeficiency 39		Search Ontology:
Synonyms:	IMD39
Definition:	A primary immunodeficiency disease characterized by impaired interferon I and III production in response to influenza virus infection that has_material_basis_in homozygous or compond heterozygous mutation in the IRF7 gene on chromosome 11p15.5. https://pubmed.ncbi.nlm.nih.gov/25814066/
References:	OMIM:616345
Ontology:	Human Disease ( DOID:0111969 )

Relationships

is a type of:	autosomal dominant disease primary immunodeficiency disease autosomal dominant disease primary immunodeficiency disease Show first 5 Terms

OTHER immunodeficiency 39 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
IRF7	irf7	?Immunodeficiency 39	616345

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None