OBO ID: DOID:0050177 |
Term Name: | monogenic disease | Search Ontology: | |
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Synonyms: |
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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 ) |
OTHER monogenic disease PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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