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Disease Ontology Browser
adult-onset type II citrullinemia (DOID:0070342)
Alliance: disease page
Synonyms: citrin deficiency
Alt IDs: OMIM:603471
Definition: A citrullinemia that has_material_basis_in homozygous or compound heterozygous mutation in the SLC25A13 gene on chromosome 7q21.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory