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's subclass of is recorded as hereditary haemochromatosis[4].
- hemochromatosis type 5's subclass of is recorded as genetic disease[5].
- hemochromatosis type 5's MeSH descriptor ID is recorded as C565020[6].
- hemochromatosis type 5's OMIM ID is recorded as 615517[7].
- hemochromatosis type 5's Disease Ontology ID is recorded as DOID:0111031[8].
- hemochromatosis type 5's Orphanet ID is recorded as 447792[9].
- hemochromatosis type 5's Orphanet ID is recorded as 247790[10].
- hemochromatosis type 5's genetic association is recorded as FTH1[11].
- hemochromatosis type 5's Google Knowledge Graph ID is recorded as /g/11fr16jjwl[12].
- hemochromatosis type 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111031[13].
- hemochromatosis type 5's exact match is recorded as http://identifiers.org/doid/DOID:0111031[14].
- hemochromatosis type 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_247790[15].
- hemochromatosis type 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_447792[16].
- hemochromatosis type 5's UMLS CUI is recorded as C1851316[17].
- hemochromatosis type 5's UMLS CUI is recorded as CN181217[18].
- hemochromatosis type 5's ICD-10-CM is recorded as E83.1[19].
- hemochromatosis type 5's GARD rare disease ID is recorded as 13472[20].
- hemochromatosis type 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
- hemochromatosis type 5's Mondo ID is recorded as MONDO_0014225[22].
- hemochromatosis type 5's UniProt disease ID is recorded as DI-03942[23].