Search Ontology:
Human Disease

immunodeficiency 79

Term ID
DOID:0112277
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
Ontology
Human Disease   ( DOID:0112277 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models