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Summary Literature (0)
DOID:0060019 - coronin-1A deficiency

Disease Ontology Definition:A severe combined immunodeficiency that is an actin regulator when mutated results in SCID through inhibition of thymic egress of mature thymocytes into peripheral lymphoid organs.

Synonyms:

Xenbase Genes : coro1a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014168 - severe combined immunodeficiency due to CORO1A deficiency


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): severe combined immunodeficiency (is_a)