OBO ID: DOID:0060019
Term Name: coronin-1A deficiency Search Ontology:
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 coronin-1A deficiency PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CORO1A Immunodeficiency 8 615401
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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