Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0016363> ?p ?o ?g. }
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- MONDO_0016363 IAO_0000115 "OBSOLETE. Rare hereditary hemochromatosis comprises the rare forms of hereditary hemochromatosis (HH), a group of diseases characterized by excessive tissue iron deposition. These rare forms are hemochromatosis type 2 (juvenile), type 3 (TFR2-related), and type 4 (ferroportin disease). Hemochromatosis type 1 (also called classic hemochromatosis) is not a rare disease." @default.
- MONDO_0016363 IAO_0000233 "https://github.com/monarch-initiative/mondo/issues/254" @default.
- MONDO_0016363 IAO_0100001 "MONDO:0006507" @default.
- MONDO_0016363 normalizedInformationContent "100" @default.
- MONDO_0016363 referenceCount "1" @default.
- MONDO_0016363 hasBroadSynonym "iron overload disease" @default.
- MONDO_0016363 hasDbXref "GARD:20540" @default.
- MONDO_0016363 hasDbXref "ICD9:275.01" @default.
- MONDO_0016363 hasDbXref "NCIT:C84764" @default.
- MONDO_0016363 hasDbXref "Orphanet:220489" @default.
- MONDO_0016363 hasExactSynonym "rare hereditary hemochromatosis" @default.
- MONDO_0016363 id "MONDO:0016363" @default.
- MONDO_0016363 inSubset disease_grouping @default.
- MONDO_0016363 inSubset gard_rare @default.
- MONDO_0016363 inSubset ordo_disease @default.
- MONDO_0016363 inSubset ordo_group_of_disorders @default.
- MONDO_0016363 inSubset rare @default.
- MONDO_0016363 type Class @default.
- MONDO_0016363 isDefinedBy mondo.owl @default.
- MONDO_0016363 label "obsolete rare hereditary hemochromatosis" @default.
- MONDO_0016363 subClassOf MONDO_0016363 @default.
- MONDO_0016363 subClassOf Thing @default.
- MONDO_0016363 deprecated "true" @default.
- MONDO_0016363 exactMatch Orphanet_220489 @default.