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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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http://purl.obolibrary.org/obo/DOID_0050177 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_0050177 BioAssay Ontology / 生物活性分析本体 SAME_URI
http://purl.obolibrary.org/obo/DOID_0050177 Cell Line Ontology Subset for Chinese National Infrastructure of Cell Line Resource (NICR) / 国家实验细胞资源共享服务平台(NICR)细胞系本体子集 SAME_URI
http://purl.obolibrary.org/obo/DOID_0050177 细胞系本体（中文翻译） / Cell Line Ontology (Chinese Translation) SAME_URI
http://purl.obolibrary.org/obo/DOID_0050177 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/DOID_0050177 Human Disease Ontology / 人类疾病本体 SAME_URI