autoimmune lymphoproliferative syndrome type 2A

Summary

DOID:0110115 - autoimmune lymphoproliferative syndrome type 2A

Disease Ontology Definition:An autoimmune lymphoproliferative syndrome that has_material_basis_in mutation in the CASP10 gene.

Synonyms: ALPS2A, autoimmune lymphoproliferative syndrome type IIA

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

: casp10

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011383 - autoimmune lymphoproliferative syndrome type 2A

MONDO:0011383 - autoimmune lymphoproliferative syndrome type 2A

MIM:

MIM:603909 - AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA; ALPS2A

MIM:603909 - AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA; ALPS2A

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

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

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