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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0011147> ?p ?o ?g. }

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MONDO_0011147 disease_has_major_feature COB_0000033 @default.
MONDO_0011147 disease_has_major_feature COB_0000111 @default.
MONDO_0011147 disease_has_major_feature COB_0000502 @default.
MONDO_0011147 disease_has_major_feature MONDO_0000001 @default.
MONDO_0011147 disease_has_major_feature MONDO_0001176 @default.
MONDO_0011147 disease_has_major_feature MONDO_0002022 @default.
MONDO_0011147 disease_has_major_feature MONDO_0003847 @default.
MONDO_0011147 disease_has_major_feature MONDO_0005129 @default.
MONDO_0011147 disease_has_major_feature MONDO_0005328 @default.
MONDO_0011147 disease_has_major_feature MONDO_0024458 @default.
MONDO_0011147 disease_has_major_feature MONDO_0700096 @default.
MONDO_0011147 disease_has_major_feature OGMS_0000031 @default.
MONDO_0011147 disease_has_major_feature PATO_0000001 @default.
MONDO_0011147 excluded_subClassOf MONDO_0005027 @default.
MONDO_0011147 excluded_subClassOf MONDO_0015501 @default.
MONDO_0011147 excluded_subClassOf MONDO_0020226 @default.
MONDO_0011147 normalizedInformationContent "92.730304365937428" @default.
MONDO_0011147 referenceCount "3" @default.
MONDO_0011147 hasDbXref "DOID:0060407" @default.
MONDO_0011147 hasDbXref "GARD:10865" @default.
MONDO_0011147 hasDbXref "GARD:20837" @default.
MONDO_0011147 hasDbXref "ICD9:758.39" @default.
MONDO_0011147 hasDbXref "MESH:C536580" @default.
MONDO_0011147 hasDbXref "NCIT:C84522" @default.
MONDO_0011147 hasDbXref "OMIM:601808" @default.
MONDO_0011147 hasDbXref "Orphanet:1600" @default.
MONDO_0011147 hasDbXref "Orphanet:262146" @default.
MONDO_0011147 hasDbXref "SCTID:270889005" @default.
MONDO_0011147 hasDbXref "UMLS:C0432443" @default.
MONDO_0011147 hasExactSynonym "18Q syndrome" @default.
MONDO_0011147 hasExactSynonym "18q deletion syndrome" @default.
MONDO_0011147 hasExactSynonym "18q-syndrome" @default.
MONDO_0011147 hasExactSynonym "chromosome 18q deletion syndrome" @default.
MONDO_0011147 hasExactSynonym "deletion 18q syndrome" @default.
MONDO_0011147 hasExactSynonym "deletion 18q" @default.
MONDO_0011147 hasExactSynonym "monosomy 18q" @default.
MONDO_0011147 hasExactSynonym "monosomy type 18q" @default.
MONDO_0011147 hasExactSynonym "partial deletion of chromosome 18q" @default.
MONDO_0011147 hasExactSynonym "partial deletion of the long arm of chromosome 18" @default.
MONDO_0011147 hasExactSynonym "partial deletion of the long arm of chromosome type 18" @default.
MONDO_0011147 hasExactSynonym "partial monosomy of chromosome 18q" @default.
MONDO_0011147 hasExactSynonym "partial monosomy of the long arm of chromosome 18" @default.
MONDO_0011147 hasNarrowSynonym "proximal 18q deletion syndrome" @default.
MONDO_0011147 hasNarrowSynonym "proximal 18q deletion" @default.
MONDO_0011147 hasNarrowSynonym "proximal 18q-" @default.
MONDO_0011147 hasNarrowSynonym "proximal chromosome 18q deletion syndrome" @default.
MONDO_0011147 hasRelatedSynonym "18Q- syndrome" @default.
MONDO_0011147 hasRelatedSynonym "chromosome 18Q- syndrome" @default.
MONDO_0011147 hasRelatedSynonym "chromosome 18q deletion" @default.
MONDO_0011147 hasRelatedSynonym "monosomy 18q syndrome" @default.
MONDO_0011147 id "MONDO:0011147" @default.
MONDO_0011147 inSubset disease_grouping @default.
MONDO_0011147 inSubset gard_rare @default.
MONDO_0011147 inSubset nord_rare @default.
MONDO_0011147 inSubset ordo_malformation_syndrome @default.
MONDO_0011147 inSubset orphanet_rare @default.
MONDO_0011147 inSubset rare @default.
MONDO_0011147 type Class @default.
MONDO_0011147 isDefinedBy mondo.owl @default.
MONDO_0011147 label "chromosome 18q deletion syndrome" @default.
MONDO_0011147 subClassOf B0e2c124e27c86901815d859a25934d9e @default.
MONDO_0011147 subClassOf B7614432a0d8fc91c9edb962470b55920 @default.
MONDO_0011147 subClassOf B982e1163acd4ddf66cab257060d6b48f @default.
MONDO_0011147 subClassOf Bf7f5f391789e1fad88f2223c2600b027 @default.
MONDO_0011147 subClassOf BFO_0000001 @default.
MONDO_0011147 subClassOf BFO_0000002 @default.
MONDO_0011147 subClassOf BFO_0000016 @default.
MONDO_0011147 subClassOf BFO_0000017 @default.
MONDO_0011147 subClassOf BFO_0000020 @default.
MONDO_0011147 subClassOf COB_0000033 @default.
MONDO_0011147 subClassOf COB_0000111 @default.
MONDO_0011147 subClassOf COB_0000502 @default.
MONDO_0011147 subClassOf MONDO_0000001 @default.
MONDO_0011147 subClassOf MONDO_0000761 @default.
MONDO_0011147 subClassOf MONDO_0002254 @default.
MONDO_0011147 subClassOf MONDO_0011147 @default.
MONDO_0011147 subClassOf MONDO_0016880 @default.
MONDO_0011147 subClassOf MONDO_0019040 @default.
MONDO_0011147 subClassOf MONDO_0020049 @default.
MONDO_0011147 subClassOf MONDO_0700096 @default.
MONDO_0011147 subClassOf MONDO_0700125 @default.
MONDO_0011147 subClassOf OGMS_0000031 @default.
MONDO_0011147 subClassOf PATO_0000001 @default.
MONDO_0011147 equivalentClass B87494dbc5d677aa3d37752ff3b13f145 @default.
MONDO_0011147 equivalentClass B8b081abaa1f0868b9c772e90d3630fba @default.
MONDO_0011147 exactMatch NCIT_C84522 @default.
MONDO_0011147 exactMatch C536580 @default.
MONDO_0011147 exactMatch 270889005 @default.
MONDO_0011147 exactMatch C0432443 @default.
MONDO_0011147 exactMatch DOID_0060407 @default.
MONDO_0011147 exactMatch Orphanet_1600 @default.
MONDO_0011147 exactMatch Orphanet_262146 @default.
MONDO_0011147 exactMatch 601808 @default.
MONDO_0011147 category Attribute @default.
MONDO_0011147 category BiologicalEntity @default.
MONDO_0011147 category Disease @default.
MONDO_0011147 category DiseaseOrPhenotypicFeature @default.
MONDO_0011147 category Entity @default.
MONDO_0011147 category NamedThing @default.
MONDO_0011147 category OntologyClass @default.

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