hemochromatosis type 5
hemochromatosis that has material basis in heterozygous mutation in the FTH1 gene on chromosome 11q12
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hemochromatosis type 5
Summary
hemochromatosis type 5 is a rare disease[1].
Key Facts
- hemochromatosis type 5's instance of is recorded as rare disease[2].
- hemochromatosis type 5's instance of is recorded as class of disease[3].
- hemochromatosis type 5 is a type of hereditary haemochromatosis[4].
- hemochromatosis type 5 is a type of genetic disease[5].
- hemochromatosis type 5's genetic association is recorded as FTH1[6].
- hemochromatosis type 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111031[7].
- hemochromatosis type 5's exact match is recorded as http://identifiers.org/doid/DOID:0111031[8].
- hemochromatosis type 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_247790[9].
- hemochromatosis type 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_447792[10].
- hemochromatosis type 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].