autoimmune lymphoproliferative syndrome type 3

Summary

DOID:0110119 - autoimmune lymphoproliferative syndrome type 3

Disease Ontology Definition:An autoimmune lymphoproliferative syndrome that has_material_basis_in homozygous mutation in the PRKCD gene on chromosome 3p21.

Synonyms: ALPS3, CVID9, autoimmune lymphoproliferative syndrome type III, common variable immunodeficiency 9,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: prkcd

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014253 - obsolete autoimmune lymphoproliferative syndrome type 3

MONDO:0014253 - obsolete autoimmune lymphoproliferative syndrome type 3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autoimmune lymphoproliferative syndrome (is_a), autosomal recessive disease (is_a)