Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0007779> ?p ?o ?g. }
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- MONDO_0007779 IAO_0000115 "OBSOLETE. Autosomal dominant form of Opitz G/BBB syndrome." @default.
- MONDO_0007779 IAO_0000231 OMO_0001000 @default.
- MONDO_0007779 IAO_0000233 "https://github.com/monarch-initiative/mondo/issues/6312" @default.
- MONDO_0007779 normalizedInformationContent "100" @default.
- MONDO_0007779 referenceCount "1" @default.
- MONDO_0007779 consider "MONDO:0800025" @default.
- MONDO_0007779 hasDbXref "OMIM:145410" @default.
- MONDO_0007779 hasDbXref "Orphanet:306588" @default.
- MONDO_0007779 hasExactSynonym "ADOS" @default.
- MONDO_0007779 hasExactSynonym "Opitz G/BBB syndrome, autosomal dominant" @default.
- MONDO_0007779 hasExactSynonym "autosomal dominant Opitz BBB/G syndrome" @default.
- MONDO_0007779 hasExactSynonym "autosomal dominant Opitz syndrome" @default.
- MONDO_0007779 hasRelatedSynonym "BBB syndrome" @default.
- MONDO_0007779 hasRelatedSynonym "G syndrome" @default.
- MONDO_0007779 hasRelatedSynonym "GBBB syndrome" @default.
- MONDO_0007779 hasRelatedSynonym "GBBB2" @default.
- MONDO_0007779 hasRelatedSynonym "Opitz Bbbg syndrome" @default.
- MONDO_0007779 hasRelatedSynonym "Opitz GBBB syndrome, autosomal dominant" @default.
- MONDO_0007779 hasRelatedSynonym "Opitz GBBB syndrome, type 2" @default.
- MONDO_0007779 hasRelatedSynonym "Opitz GBBB syndrome, type II" @default.
- MONDO_0007779 hasRelatedSynonym "Opitz oculogenitolaryngeal syndrome, type 2" @default.
- MONDO_0007779 hasRelatedSynonym "Opitz-Frias syndrome" @default.
- MONDO_0007779 hasRelatedSynonym "Opitz-G syndrome, type 2" @default.
- MONDO_0007779 hasRelatedSynonym "chromosome 22Q11.2 deletion syndrome, Opitz phenotype" @default.
- MONDO_0007779 hasRelatedSynonym "hypertelorism with esophageal Abnormality and hypospadias" @default.
- MONDO_0007779 hasRelatedSynonym "hypertelorism-hypospadias syndrome" @default.
- MONDO_0007779 hasRelatedSynonym "hypospadias-dysphagia syndrome" @default.
- MONDO_0007779 hasRelatedSynonym "telecanthus with associated abnormalities" @default.
- MONDO_0007779 hasRelatedSynonym "telecanthus-hypospadias syndrome" @default.
- MONDO_0007779 id "MONDO:0007779" @default.
- MONDO_0007779 inSubset ordo_etiological_subtype @default.
- MONDO_0007779 type Class @default.
- MONDO_0007779 isDefinedBy mondo.owl @default.
- MONDO_0007779 label "obsolete autosomal dominant Opitz G/BBB syndrome" @default.
- MONDO_0007779 subClassOf MONDO_0007779 @default.
- MONDO_0007779 subClassOf Thing @default.
- MONDO_0007779 deprecated "true" @default.
- MONDO_0007779 exactMatch Orphanet_306588 @default.
- MONDO_0007779 exactMatch 145410 @default.