ZFIN Human Disease: immunodeficiency 45

OBO ID: DOID:0111994

Term Name:	immunodeficiency 45		Search Ontology:
Synonyms:	IMD45
Definition:	A primary immunodeficiency disease characterized by impaired control the replication of certain viruses and failure to develop an antiviral state in response to alpha-interferon or beta-interferon that has_material_basis_in homozygous or compound heterozygous mutation in the IFNAR2 gene on chromosome 21q22.11. https://pubmed.ncbi.nlm.nih.gov/26424569/
References:	OMIM:616669
Ontology:	Human Disease ( DOID:0111994 )

Relationships

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

OTHER immunodeficiency 45 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
IFNAR2		Immunodeficiency 45

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None