DISEASES

Disease-gene associations mined from literature

Human genes for coronin-1A deficiency

coronin-1A deficiency [DOID:0060019]

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:  coronin-1A deficiency,  DOID:0060019,  coronin1A deficiency