Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0015969> ?p ?o ?g. }
Showing items 1 to 22 of
22
with 100 items per page.
- MONDO_0015969 IAO_0000115 "OBSOLETE. Rare genetic thyroid disease." @default.
- MONDO_0015969 IAO_0000233 "https://github.com/monarch-initiative/mondo/issues/254" @default.
- MONDO_0015969 IAO_0100001 "MONDO:0003240" @default.
- MONDO_0015969 normalizedInformationContent "100" @default.
- MONDO_0015969 referenceCount "1" @default.
- MONDO_0015969 hasDbXref "GARD:20314" @default.
- MONDO_0015969 hasDbXref "Orphanet:183631" @default.
- MONDO_0015969 hasDbXref "UMLS:CN200568" @default.
- MONDO_0015969 hasExactSynonym "rare genetic thyroid disease" @default.
- MONDO_0015969 id "MONDO:0015969" @default.
- MONDO_0015969 inSubset disease_grouping @default.
- MONDO_0015969 inSubset gard_rare @default.
- MONDO_0015969 inSubset ordo_group_of_disorders @default.
- MONDO_0015969 inSubset rare @default.
- MONDO_0015969 type Class @default.
- MONDO_0015969 isDefinedBy mondo.owl @default.
- MONDO_0015969 label "obsolete rare genetic thyroid disease" @default.
- MONDO_0015969 subClassOf MONDO_0015969 @default.
- MONDO_0015969 subClassOf Thing @default.
- MONDO_0015969 deprecated "true" @default.
- MONDO_0015969 exactMatch CN200568 @default.
- MONDO_0015969 exactMatch Orphanet_183631 @default.