Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0008047> ?p ?o ?g. }
- MONDO_0008047 disease_has_major_feature PATO_0000161 @default.
- MONDO_0008047 disease_has_major_feature PATO_0000186 @default.
- MONDO_0008047 disease_has_major_feature PATO_0000188 @default.
- MONDO_0008047 disease_has_major_feature PATO_0000911 @default.
- MONDO_0008047 disease_has_major_feature PATO_0001236 @default.
- MONDO_0008047 disease_has_major_feature PATO_0001241 @default.
- MONDO_0008047 disease_has_major_feature PATO_0001509 @default.
- MONDO_0008047 disease_has_major_feature PATO_0001995 @default.
- MONDO_0008047 disease_has_major_feature PATO_0002062 @default.
- MONDO_0008047 disease_has_major_feature PATO_0002301 @default.
- MONDO_0008047 disease_has_major_feature PATO_0002302 @default.
- MONDO_0008047 disease_has_major_feature TO_0000283 @default.
- MONDO_0008047 disease_has_major_feature TO_0000387 @default.
- MONDO_0008047 disease_has_major_feature UPHENO_0001001 @default.
- MONDO_0008047 disease_has_major_feature WBPhenotype_0000517 @default.
- MONDO_0008047 disease_has_major_feature WBPhenotype_0000519 @default.
- MONDO_0008047 disease_has_major_feature WBPhenotype_0000886 @default.
- MONDO_0008047 normalizedInformationContent "100" @default.
- MONDO_0008047 referenceCount "1" @default.
- MONDO_0008047 hasDbXref "DOID:0050989" @default.
- MONDO_0008047 hasDbXref "GARD:16641" @default.
- MONDO_0008047 hasDbXref "OMIM:160120" @default.
- MONDO_0008047 hasDbXref "Orphanet:37612" @default.
- MONDO_0008047 hasDbXref "Orphanet:972" @default.
- MONDO_0008047 hasDbXref "SCTID:421182009" @default.
- MONDO_0008047 hasDbXref "UMLS:C1719788" @default.
- MONDO_0008047 hasDbXref "UMLS:C1834559" @default.
- MONDO_0008047 hasDbXref "UMLS:CN042654" @default.
- MONDO_0008047 hasExactSynonym "KCNA1 hereditary episodic ataxia" @default.
- MONDO_0008047 hasExactSynonym "acetazolamide-responsive periodic ataxia" @default.
- MONDO_0008047 hasExactSynonym "continuous muscle fiber activity" @default.
- MONDO_0008047 hasExactSynonym "continuous muscle fibre activity" @default.
- MONDO_0008047 hasExactSynonym "episodic ataxia with myokymia" @default.
- MONDO_0008047 hasExactSynonym "episodic ataxia/myokymia syndrome" @default.
- MONDO_0008047 hasExactSynonym "familial paroxysmal kinesigenic ataxia and continuous myokymia" @default.
- MONDO_0008047 hasExactSynonym "hereditary episodic ataxia caused by mutation in KCNA1" @default.
- MONDO_0008047 hasExactSynonym "hereditary paroxysmal ataxia with neuromyotonia" @default.
- MONDO_0008047 hasRelatedSynonym "EA1" @default.
- MONDO_0008047 hasRelatedSynonym "Isaacs-Mertens syndrome" @default.
- MONDO_0008047 hasRelatedSynonym "ataxia, episodic, with myokymia" @default.
- MONDO_0008047 hasRelatedSynonym "continuous muscle fiber activity, hereditary" @default.
- MONDO_0008047 hasRelatedSynonym "continuous muscle fibre activity, hereditary" @default.
- MONDO_0008047 hasRelatedSynonym "episodic ataxia, type 1" @default.
- MONDO_0008047 hasRelatedSynonym "myokymia 1 with or without hypomagnesemia" @default.
- MONDO_0008047 hasRelatedSynonym "myokymia 1" @default.
- MONDO_0008047 hasRelatedSynonym "myokymia with periodic ataxia" @default.
- MONDO_0008047 hasRelatedSynonym "paroxysmal ataxia with neuromyotonia, hereditary" @default.
- MONDO_0008047 id "MONDO:0008047" @default.
- MONDO_0008047 inSubset gard_rare @default.
- MONDO_0008047 inSubset nord_rare @default.
- MONDO_0008047 inSubset ordo_disease @default.
- MONDO_0008047 inSubset orphanet_rare @default.
- MONDO_0008047 inSubset rare @default.
- MONDO_0008047 type Class @default.
- MONDO_0008047 isDefinedBy mondo.owl @default.
- MONDO_0008047 label "episodic ataxia type 1" @default.
- MONDO_0008047 subClassOf B8e48c1b4d5a359a9fc99b8a11ae2ba8b @default.
- MONDO_0008047 subClassOf Bf0c69bdbd6200df5e60616e955431f70 @default.
- MONDO_0008047 subClassOf BFO_0000001 @default.
- MONDO_0008047 subClassOf BFO_0000002 @default.
- MONDO_0008047 subClassOf BFO_0000016 @default.
- MONDO_0008047 subClassOf BFO_0000017 @default.
- MONDO_0008047 subClassOf BFO_0000020 @default.
- MONDO_0008047 subClassOf COB_0000033 @default.
- MONDO_0008047 subClassOf COB_0000111 @default.
- MONDO_0008047 subClassOf COB_0000502 @default.
- MONDO_0008047 subClassOf MONDO_0000001 @default.
- MONDO_0008047 subClassOf MONDO_0003620 @default.
- MONDO_0008047 subClassOf MONDO_0003847 @default.
- MONDO_0008047 subClassOf MONDO_0005071 @default.
- MONDO_0008047 subClassOf MONDO_0005244 @default.
- MONDO_0008047 subClassOf MONDO_0008047 @default.
- MONDO_0008047 subClassOf MONDO_0016227 @default.
- MONDO_0008047 subClassOf MONDO_0019056 @default.
- MONDO_0008047 subClassOf MONDO_0020127 @default.
- MONDO_0008047 subClassOf MONDO_0100308 @default.
- MONDO_0008047 subClassOf MONDO_0100309 @default.
- MONDO_0008047 subClassOf MONDO_0700096 @default.
- MONDO_0008047 subClassOf OGMS_0000031 @default.
- MONDO_0008047 subClassOf PATO_0000001 @default.
- MONDO_0008047 equivalentClass B57c19ac00f05cdc417d01a3b91935f95 @default.
- MONDO_0008047 equivalentClass Bd4525d7fd1bfb1f31bb226041ca7465a @default.
- MONDO_0008047 exactMatch 421182009 @default.
- MONDO_0008047 exactMatch C1719788 @default.
- MONDO_0008047 exactMatch CN042654 @default.
- MONDO_0008047 exactMatch DOID_0050989 @default.
- MONDO_0008047 exactMatch Orphanet_37612 @default.
- MONDO_0008047 exactMatch 160120 @default.
- MONDO_0008047 category Attribute @default.
- MONDO_0008047 category BiologicalEntity @default.
- MONDO_0008047 category Disease @default.
- MONDO_0008047 category DiseaseOrPhenotypicFeature @default.
- MONDO_0008047 category Entity @default.
- MONDO_0008047 category NamedThing @default.
- MONDO_0008047 category OntologyClass @default.
- MONDO_0008047 category OrganismAttribute @default.
- MONDO_0008047 category PhenotypicQuality @default.
- MONDO_0008047 category ThingWithTaxon @default.