Matches in Ubergraph for { <http://purl.obolibrary.org/obo/HP_0100775> ?p ?o ?g. }
- HP_0100775 UPHENO_0000001 UBERON_0001137 @default.
- HP_0100775 UPHENO_0000001 UBERON_0002240 @default.
- HP_0100775 UPHENO_0000001 UBERON_0002360 @default.
- HP_0100775 UPHENO_0000001 UBERON_0003103 @default.
- HP_0100775 UPHENO_0000001 UBERON_0003292 @default.
- HP_0100775 UPHENO_0000001 UBERON_0004121 @default.
- HP_0100775 UPHENO_0000001 UBERON_0005174 @default.
- HP_0100775 UPHENO_0000001 UBERON_0010000 @default.
- HP_0100775 UPHENO_0000001 UBERON_0010314 @default.
- HP_0100775 UPHENO_0000001 UBERON_0010743 @default.
- HP_0100775 UPHENO_0000001 UBERON_0011216 @default.
- HP_0100775 UPHENO_0000001 UBERON_0034925 @default.
- HP_0100775 creator 0009-0006-4530-3154 @default.
- HP_0100775 normalizedInformationContent "100" @default.
- HP_0100775 referenceCount "1" @default.
- HP_0100775 creation_date "2011-06-07T05:22:13Z" @default.
- HP_0100775 hasDbXref "UMLS:C1851712" @default.
- HP_0100775 id "HP:0100775" @default.
- HP_0100775 type Class @default.
- HP_0100775 comment "Dural ectasia is one of the major manifestations of Marfan syndrome. It may cause low back pain, headaches and neurological signs such as weakness and loss of bowel and bladder function, but in many patients it is asymptomatic. It is also a cause of posterior vertebral scalloping present in radiographs in patients who are diagnosed with Neurofibromatosis. Dural ectasia may also manifest in Ehlers-Danlos Syndrome, cauda equina syndrome and in ankylosing spondylitis." @default.
- HP_0100775 isDefinedBy hp.owl @default.
- HP_0100775 label "Dural ectasia" @default.
- HP_0100775 subClassOf BFO_0000001 @default.
- HP_0100775 subClassOf BFO_0000002 @default.
- HP_0100775 subClassOf BFO_0000020 @default.
- HP_0100775 subClassOf COB_0000502 @default.
- HP_0100775 subClassOf FBcv_0000000 @default.
- HP_0100775 subClassOf FBcv_0000013 @default.
- HP_0100775 subClassOf FBcv_0000347 @default.
- HP_0100775 subClassOf FBcv_0000807 @default.
- HP_0100775 subClassOf FBcv_0001347 @default.
- HP_0100775 subClassOf HP_0000001 @default.
- HP_0100775 subClassOf HP_0000118 @default.
- HP_0100775 subClassOf HP_0000707 @default.
- HP_0100775 subClassOf HP_0002011 @default.
- HP_0100775 subClassOf HP_0002143 @default.
- HP_0100775 subClassOf HP_0010303 @default.
- HP_0100775 subClassOf HP_0010651 @default.
- HP_0100775 subClassOf HP_0012639 @default.
- HP_0100775 subClassOf HP_0100775 @default.
- HP_0100775 subClassOf MP_0000001 @default.
- HP_0100775 subClassOf MP_0000955 @default.
- HP_0100775 subClassOf MP_0003631 @default.
- HP_0100775 subClassOf MP_0003632 @default.
- HP_0100775 subClassOf MP_0005623 @default.
- HP_0100775 subClassOf MP_0009023 @default.
- HP_0100775 subClassOf PATO_0000001 @default.
- HP_0100775 subClassOf UPHENO_0001001 @default.
- HP_0100775 category Attribute @default.
- HP_0100775 category BiologicalEntity @default.
- HP_0100775 category DiseaseOrPhenotypicFeature @default.
- HP_0100775 category Entity @default.
- HP_0100775 category NamedThing @default.
- HP_0100775 category OntologyClass @default.
- HP_0100775 category OrganismAttribute @default.
- HP_0100775 category PathologicalEntityMixin @default.
- HP_0100775 category PhenotypicFeature @default.
- HP_0100775 category PhenotypicQuality @default.
- HP_0100775 category ThingWithTaxon @default.