Search Ontology:
Human Disease

monogenic disease

Term ID
DOID:0050177
Synonyms
Definition
A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive. https://www.genome.gov/For-Patients-and-Families/Genetic-Disorders
References
Ontology
Human Disease   ( DOID:0050177 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models