hemochromatosis type 3 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

hemochromatosis type 3 (DOID:0111030)
Alliance: disease page
Synonyms: hemochromatosis due to defect in transferrin receptor 2; HFE3; TFR2-related hemochromatosis
Alt IDs: OMIM:604250, MESH:C537248, ORDO:225123, UMLS_CUI:C1858664
Definition: A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22.

Disease References using Mouse Models (2)

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 04/09/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Tfr2tm1Slu/Tfr2tm1Slu	involves: 129X1/SvJ * C57BL/6J	J:78360	View
Tfr2tm1.1Anro/Tfr2tm1.1Anro	129.Cg-Tfr2^tm1.1Anro	J:160785	View