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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:
Echinobase Genes :
MIM:615401 - immunodeficiency 8; imd8 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
severe combined immunodeficiency (is_a)