hemochromatosis type 2B
hemochromatosis type 2 that has material basis in homozygous mutation in the HAMP gene on chromosome 19q13
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hemochromatosis type 2B
Summary
hemochromatosis type 2B is a class of disease[1].
Key Facts
- hemochromatosis type 2B's instance of is recorded as class of disease[2].
- hemochromatosis type 2B's subclass of is recorded as hemochromatosis type 2[3].
- hemochromatosis type 2B's subclass of is recorded as genetic disease[4].
- hemochromatosis type 2B's MeSH descriptor ID is recorded as C566557[5].
- hemochromatosis type 2B's OMIM ID is recorded as 613313[6].
- hemochromatosis type 2B's OMIM ID is recorded as 613313[7].
- hemochromatosis type 2B's Disease Ontology ID is recorded as DOID:0111032[8].
- hemochromatosis type 2B's genetic association is recorded as HAMP[9].
- hemochromatosis type 2B's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111032[10].
- hemochromatosis type 2B's exact match is recorded as http://identifiers.org/doid/DOID:0111032[11].
- hemochromatosis type 2B's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79230[12].
- hemochromatosis type 2B's UMLS CUI is recorded as C1865616[13].
- hemochromatosis type 2B's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- hemochromatosis type 2B's Mondo ID is recorded as MONDO_0013220[15].
- hemochromatosis type 2B's UniProt disease ID is recorded as DI-01700[16].