International Classification of Diseases Ontology - monogenic disease - Classes

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.
ID	http://purl.obolibrary.org/obo/DOID_0050177
has_obo_namespace	disease_ontology
id	DOID:0050177
imported from	http://purl.obolibrary.org/obo/doid.owl
in subset	http://purl.oboInOwllibrary.org/oboInOwl/doid#DO_AGR_slim http://purl.oboInOwllibrary.org/oboInOwl/doid#DO_GXD_slim
label	monogenic disease
notation	DOID:0050177
prefLabel	monogenic disease
textual definition	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

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_0050177	Cell Line Ontology Subset for Chinese National Infrastructure of Cell Line Resource (NICR)	SAME_URI
http://purl.obolibrary.org/obo/DOID_0050177	Cell Line Ontology (Chinese Translation)	SAME_URI
http://purl.obolibrary.org/obo/DOID_0050177	Human Disease Ontology 123	LOOM
http://purl.obolibrary.org/obo/DOID_0050177	Human Disease Ontology 123	SAME_URI