hemochromatosis type 1
hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22
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hemochromatosis type 1
Summary
hemochromatosis type 1 is a class of disease[1].
Key Facts
- hemochromatosis type 1's instance of is recorded as class of disease[2].
- hemochromatosis type 1's subclass of is recorded as hereditary haemochromatosis[3].
- hemochromatosis type 1's subclass of is recorded as genetic disease[4].
- hemochromatosis type 1's OMIM ID is recorded as 235200[5].
- hemochromatosis type 1's Disease Ontology ID is recorded as DOID:0111029[6].
- hemochromatosis type 1's Orphanet ID is recorded as 465508[7].
- hemochromatosis type 1's NCI Thesaurus ID is recorded as C84764[8].
- hemochromatosis type 1's genetic association is recorded as HFE[9].
- hemochromatosis type 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111029[10].
- hemochromatosis type 1's exact match is recorded as http://identifiers.org/doid/DOID:0111029[11].
- hemochromatosis type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_465508[12].
- hemochromatosis type 1's UMLS CUI is recorded as C5679990[13].
- hemochromatosis type 1's ICD-10-CM is recorded as E83.1[14].
- hemochromatosis type 1's GARD rare disease ID is recorded as 10417[15].
- hemochromatosis type 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- hemochromatosis type 1's Mondo ID is recorded as MONDO_0021001[17].
- hemochromatosis type 1's WordLift URL is recorded as http://data.medicalrecords.com/medicalrecords/healthwise/hemochromatosis[18].
- hemochromatosis type 1's UniProt disease ID is recorded as DI-01714[19].
- hemochromatosis type 1's Experimental Factor Ontology ID is recorded as 0006513[20].