Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0009627> ?p ?o ?g. }
- MONDO_0009627 RO_0002320 NCBITaxon_9605 @default.
- MONDO_0009627 RO_0002320 NCBITaxon_9606 @default.
- MONDO_0009627 RO_0002320 OBI_0100026 @default.
- MONDO_0009627 RO_0002320 PCO_0000031 @default.
- MONDO_0009627 excluded_subClassOf MONDO_0000508 @default.
- MONDO_0009627 normalizedInformationContent "84.132738204908478" @default.
- MONDO_0009627 referenceCount "11" @default.
- MONDO_0009627 hasDbXref "DOID:0080694" @default.
- MONDO_0009627 hasDbXref "GARD:65" @default.
- MONDO_0009627 hasDbXref "MESH:C537548" @default.
- MONDO_0009627 hasDbXref "NCIT:C132195" @default.
- MONDO_0009627 hasDbXref "OMIMPS:251300" @default.
- MONDO_0009627 hasDbXref "Orphanet:2065" @default.
- MONDO_0009627 hasDbXref "SCTID:721297008" @default.
- MONDO_0009627 hasDbXref "UMLS:C0795949" @default.
- MONDO_0009627 hasExactSynonym "Galloway syndrome" @default.
- MONDO_0009627 hasExactSynonym "Galloway-Mowat syndrome" @default.
- MONDO_0009627 hasExactSynonym "microcephaly, hiatal hernia and nephrotic syndrome" @default.
- MONDO_0009627 hasExactSynonym "microcephaly-hiatus hernia-nephrotic syndrome" @default.
- MONDO_0009627 hasExactSynonym "nephrosis-microcephaly syndrome" @default.
- MONDO_0009627 hasExactSynonym "nephrosis-neuronal dysmigration syndrome" @default.
- MONDO_0009627 hasExactSynonym "spinocerebellar ataxia, autosomal recessive 5" @default.
- MONDO_0009627 hasRelatedSynonym "GAMOS" @default.
- MONDO_0009627 hasRelatedSynonym "Galloway Mowat syndrome" @default.
- MONDO_0009627 hasRelatedSynonym "cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities" @default.
- MONDO_0009627 hasRelatedSynonym "cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities" @default.
- MONDO_0009627 hasRelatedSynonym "hiatal hernia-microcephaly-nephrosis, Galloway type" @default.
- MONDO_0009627 hasRelatedSynonym "microcephaly nephrosis syndrome" @default.
- MONDO_0009627 hasRelatedSynonym "microcephaly, hiatal hernia, and nephrotic syndrome" @default.
- MONDO_0009627 hasRelatedSynonym "nephrosis neuronal dysmigration syndrome" @default.
- MONDO_0009627 hasRelatedSynonym "spinocerebellar ataxia, autosomal recessive 5, formerly" @default.
- MONDO_0009627 id "MONDO:0009627" @default.
- MONDO_0009627 inSubset gard_rare @default.
- MONDO_0009627 inSubset nord_rare @default.
- MONDO_0009627 inSubset ordo_malformation_syndrome @default.
- MONDO_0009627 inSubset orphanet_rare @default.
- MONDO_0009627 inSubset prototype_pattern @default.
- MONDO_0009627 inSubset rare @default.
- MONDO_0009627 type Class @default.
- MONDO_0009627 isDefinedBy mondo.owl @default.
- MONDO_0009627 label "Galloway-Mowat syndrome" @default.
- MONDO_0009627 subClassOf B02fa6b10b0be7fa363e71ac53db43a4c @default.
- MONDO_0009627 subClassOf Baaa88a2bad352e0a779a33ef4552e4c4 @default.
- MONDO_0009627 subClassOf BFO_0000001 @default.
- MONDO_0009627 subClassOf BFO_0000002 @default.
- MONDO_0009627 subClassOf BFO_0000016 @default.
- MONDO_0009627 subClassOf BFO_0000017 @default.
- MONDO_0009627 subClassOf BFO_0000020 @default.
- MONDO_0009627 subClassOf COB_0000033 @default.
- MONDO_0009627 subClassOf COB_0000111 @default.
- MONDO_0009627 subClassOf COB_0000502 @default.
- MONDO_0009627 subClassOf MONDO_0000001 @default.
- MONDO_0009627 subClassOf MONDO_0000429 @default.
- MONDO_0009627 subClassOf MONDO_0002254 @default.
- MONDO_0009627 subClassOf MONDO_0003847 @default.
- MONDO_0009627 subClassOf MONDO_0006025 @default.
- MONDO_0009627 subClassOf MONDO_0009627 @default.
- MONDO_0009627 subClassOf MONDO_0700096 @default.
- MONDO_0009627 subClassOf PATO_0000001 @default.
- MONDO_0009627 exactMatch NCIT_C132195 @default.
- MONDO_0009627 exactMatch C537548 @default.
- MONDO_0009627 exactMatch 721297008 @default.
- MONDO_0009627 exactMatch C0795949 @default.
- MONDO_0009627 exactMatch DOID_0080694 @default.
- MONDO_0009627 exactMatch Orphanet_2065 @default.
- MONDO_0009627 exactMatch PS251300 @default.
- MONDO_0009627 category Attribute @default.
- MONDO_0009627 category BiologicalEntity @default.
- MONDO_0009627 category Disease @default.
- MONDO_0009627 category DiseaseOrPhenotypicFeature @default.
- MONDO_0009627 category Entity @default.
- MONDO_0009627 category NamedThing @default.
- MONDO_0009627 category OntologyClass @default.
- MONDO_0009627 category OrganismAttribute @default.
- MONDO_0009627 category PhenotypicQuality @default.
- MONDO_0009627 category ThingWithTaxon @default.