Human disease ontology - genetic disease - Terms

Preferred Name	genetic disease
Definitions	A disease that has_material_basis_in genetic variations in the human genome.
ID	DOID:630
Full Id	http://purl.obolibrary.org/obo/DOID_630
xref	MSH:D030342 NCI:C3101 SNOMEDCT_2010_1_31:264530000 SNOMEDCT_2010_1_31:32895009 UMLS_CUI:C0019247
xref_definition	http://ghr.nlm.nih.gov/]
is_a	disease

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Mapping To	Ontology	Source	Relationship	Added By	Added On	Notes
http://www.owl-ontologies.com/NPOntology.owl#DOID_630	Natural Products Ontology	NCBO (lexical mapping)	skos:closeMatch	loom	05/21/13	View Notes
http://purl.obolibrary.org/obo/DOID_630	Neuroscience Information Framework Standard ontology	NCBO (Identical URI)	skos:exactMatch	loom	05/21/13	View Notes
http://www.semanticweb.org/ontologies/2010/2/MiRNA-Ontology.owl#GeneticDisease	Ontology for MicroRNA Target Prediction	NCBO (lexical mapping)	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/SNOMEDCT/32895009	SNOMED Clinical Terms	NCBO (lexical mapping)	skos:closeMatch	loom	05/21/13	View Notes

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