EpilepsyOntology

Last uploaded: November 8, 2021

Id	http://purl.obolibrary.org/obo/DOID_0050177 http://purl.obolibrary.org/obo/DOID_0050177
Preferred Name	monogenic disease
Definitions	A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.
Type	http://www.w3.org/2002/07/owl#Class

label	monogenic disease
prefLabel	monogenic disease
notation	DOID:0050177
in subset	http://purl.oboInOwllibrary.org/oboInOwl/doid#DO_AGR_slim http://purl.oboInOwllibrary.org/oboInOwl/doid#DO_GXD_slim
id	DOID:0050177
has_obo_namespace	disease_ontology
文本定义	A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.
subClassOf	http://purl.obolibrary.org/obo/DOID_630
imported from	http://purl.obolibrary.org/obo/doid.owl
type	http://www.w3.org/2002/07/owl#Class

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