Search Ontology:
Human Disease

coronin-1A deficiency

Term ID
DOID:0060019
Synonyms
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. (2)
References
Ontology
Human Disease   ( DOID:0060019 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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