ZFIN Human Disease: immunodeficiency 79

OBO ID: DOID:0112277

Term Name:	immunodeficiency 79		Search Ontology:
Synonyms:	IMD79
Definition:	A T cell deficiency characterized by childhood onset of recurrent and recalcitrant skin warts due to uncontrolled viral infection with human papillomavirus and absence of the CD4 antigen on T cells, monocytes, and dendritic cells that has_material_basis_in homozygous or compound heterozygous mutation in CD4 on chromosome 12p13. (2)
References:	OMIM:619238
Ontology:	Human Disease ( DOID:0112277 )

Relationships

is a type of:	autosomal recessive disease T cell deficiency autosomal recessive disease T cell deficiency Show first 5 Terms

OTHER immunodeficiency 79 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CD4	cd4-1	Immunodeficiency 79	619238

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None