Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0018569> ?p ?o ?g. }
- MONDO_0018569 hasDbXref "Orphanet:435938" @default.
- MONDO_0018569 hasDbXref "UMLS:CN237580" @default.
- MONDO_0018569 id "MONDO:0018569" @default.
- MONDO_0018569 inSubset gard_rare @default.
- MONDO_0018569 inSubset nord_rare @default.
- MONDO_0018569 inSubset ordo_malformation_syndrome @default.
- MONDO_0018569 inSubset orphanet_rare @default.
- MONDO_0018569 inSubset rare @default.
- MONDO_0018569 type Class @default.
- MONDO_0018569 isDefinedBy mondo.owl @default.
- MONDO_0018569 label "X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome" @default.
- MONDO_0018569 subClassOf BFO_0000001 @default.
- MONDO_0018569 subClassOf BFO_0000002 @default.
- MONDO_0018569 subClassOf BFO_0000016 @default.
- MONDO_0018569 subClassOf BFO_0000017 @default.
- MONDO_0018569 subClassOf BFO_0000020 @default.
- MONDO_0018569 subClassOf COB_0000033 @default.
- MONDO_0018569 subClassOf COB_0000111 @default.
- MONDO_0018569 subClassOf COB_0000502 @default.
- MONDO_0018569 subClassOf MONDO_0000001 @default.
- MONDO_0018569 subClassOf MONDO_0002254 @default.
- MONDO_0018569 subClassOf MONDO_0018569 @default.
- MONDO_0018569 subClassOf MONDO_0700096 @default.
- MONDO_0018569 subClassOf PATO_0000001 @default.
- MONDO_0018569 exactMatch CN237580 @default.
- MONDO_0018569 exactMatch Orphanet_435938 @default.
- MONDO_0018569 category Attribute @default.
- MONDO_0018569 category BiologicalEntity @default.
- MONDO_0018569 category Disease @default.
- MONDO_0018569 category DiseaseOrPhenotypicFeature @default.
- MONDO_0018569 category Entity @default.
- MONDO_0018569 category NamedThing @default.
- MONDO_0018569 category OntologyClass @default.
- MONDO_0018569 category OrganismAttribute @default.
- MONDO_0018569 category PhenotypicQuality @default.
- MONDO_0018569 category ThingWithTaxon @default.