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DO Term : coronin-1A deficiency [DOID:0060019] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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:
615401,
OMIM:615401

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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