OBO ID: DOID:0050177
Term Name: monogenic disease Search Ontology:
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 monogenic disease PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None