Search Ontology:
Human Disease

recombinase activating gene 1 deficiency

Term ID
DOID:0060011
Synonyms
Definition
A severe combined immunodeficiency that is the result of a mutation on Chromosome 6 RAG1 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:0060011 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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