OBO ID: DOID:0060012
Term Name: recombinase activating gene 2 deficiency Search Ontology:
Synonyms:
Definition: A severe combined immunodeficiency that is the result of a mutation on Chromosome 6 RAG2 gene involving genetic rearrangement of both the T- and B-lymphocyte receptor genes. http://medicine.jrank.org/pages/2840/Severe-Combined-Immune-Deficiency.html
References:
Ontology: Human Disease   ( DOID:0060012 )
Relationships
is a type of:
OTHER recombinase activating gene 2 deficiency PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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