xanthinuria type II Disease Ontology Browser

Home
Genes
Phenotypes
Human Disease
Expression
Recombinases
Function
Strains / SNPs
Homology
Tumors

About Help FAQ

Search
Download
More Resources
Submit Data
Find Mice (IMSR)
Analysis Tools
Contact Us
Browsers

Disease Ontology Browser

xanthinuria type II (DOID:0070453)
Alliance: disease page
Synonyms: XAN2
Alt IDs: OMIM:603592, MESH:C566358, ORDO:93602, UMLS_CUI:C1863688
Definition: A xanthinuria characterized by deficiency of xanthine dehydrogenase and aldehyde oxidase that has_material_basis_in homozygous or compound heterozygous mutation in the MOCOS gene on chromosome 18q12.

Disease References using Mouse Models (1)

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Mocosem2(IMPC)Ics/Mocosem2(IMPC)Ics	involves: C57BL/6N	J:336718	View