Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0011150> ?p ?o ?g. }
- MONDO_0011150 RO_0004024 GO_0007568 @default.
- MONDO_0011150 RO_0040035 GO_0007568 @default.
- MONDO_0011150 excluded_subClassOf MONDO_0015333 @default.
- MONDO_0011150 normalizedInformationContent "100" @default.
- MONDO_0011150 referenceCount "1" @default.
- MONDO_0011150 hasDbXref "GARD:4276" @default.
- MONDO_0011150 hasDbXref "MESH:C536653" @default.
- MONDO_0011150 hasDbXref "OMIM:601812" @default.
- MONDO_0011150 hasDbXref "Orphanet:363665" @default.
- MONDO_0011150 hasDbXref "UMLS:C1866182" @default.
- MONDO_0011150 hasExactSynonym "premature ageing syndrome, Penttinen type" @default.
- MONDO_0011150 hasExactSynonym "premature aging syndrome, Penttinen type" @default.
- MONDO_0011150 hasRelatedSynonym "PENTT" @default.
- MONDO_0011150 hasRelatedSynonym "Penttinen-aula syndrome" @default.
- MONDO_0011150 hasRelatedSynonym "premature ageing syndrome Penttinen type" @default.
- MONDO_0011150 hasRelatedSynonym "premature aging syndrome Penttinen type" @default.
- MONDO_0011150 hasRelatedSynonym "prematurely aged appearance, delayed bone maturation, acro-osteolysis, and brachydactyly" @default.
- MONDO_0011150 hasRelatedSynonym "progeroid syndrome, Penttinen type" @default.
- MONDO_0011150 id "MONDO:0011150" @default.
- MONDO_0011150 inSubset gard_rare @default.
- MONDO_0011150 inSubset nord_rare @default.
- MONDO_0011150 inSubset ordo_disease @default.
- MONDO_0011150 inSubset orphanet_rare @default.
- MONDO_0011150 inSubset rare @default.
- MONDO_0011150 type Class @default.
- MONDO_0011150 isDefinedBy mondo.owl @default.
- MONDO_0011150 label "acroosteolysis-keloid-like lesions-premature aging syndrome" @default.
- MONDO_0011150 subClassOf Ba60501d14cb8c236b53573c410453284 @default.
- MONDO_0011150 subClassOf Bc6377af857477a26300140d5a1eb314e @default.
- MONDO_0011150 subClassOf BFO_0000001 @default.
- MONDO_0011150 subClassOf BFO_0000002 @default.
- MONDO_0011150 subClassOf BFO_0000016 @default.
- MONDO_0011150 subClassOf BFO_0000017 @default.
- MONDO_0011150 subClassOf BFO_0000020 @default.
- MONDO_0011150 subClassOf COB_0000033 @default.
- MONDO_0011150 subClassOf COB_0000111 @default.
- MONDO_0011150 subClassOf COB_0000502 @default.
- MONDO_0011150 subClassOf MONDO_0000001 @default.
- MONDO_0011150 subClassOf MONDO_0011150 @default.
- MONDO_0011150 subClassOf MONDO_0019303 @default.
- MONDO_0011150 subClassOf MONDO_0700096 @default.
- MONDO_0011150 subClassOf OGMS_0000031 @default.
- MONDO_0011150 subClassOf PATO_0000001 @default.
- MONDO_0011150 exactMatch C536653 @default.
- MONDO_0011150 exactMatch C1866182 @default.
- MONDO_0011150 exactMatch Orphanet_363665 @default.
- MONDO_0011150 exactMatch 601812 @default.
- MONDO_0011150 category Attribute @default.
- MONDO_0011150 category BiologicalEntity @default.
- MONDO_0011150 category Disease @default.
- MONDO_0011150 category DiseaseOrPhenotypicFeature @default.
- MONDO_0011150 category Entity @default.
- MONDO_0011150 category NamedThing @default.
- MONDO_0011150 category OntologyClass @default.
- MONDO_0011150 category OrganismAttribute @default.
- MONDO_0011150 category PhenotypicQuality @default.
- MONDO_0011150 category ThingWithTaxon @default.