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Summary Literature (0)
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: CVID9, common variable immunodeficiency 9, ALPS3, autoimmune lymphoproliferative syndrome type III

Xenbase Genes : prkcd

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014253 - obsolete autoimmune lymphoproliferative syndrome type 3

MIM:
MIM:615559 - AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): autoimmune lymphoproliferative syndrome (is_a), autosomal recessive disease (is_a)