What is another word for monogenic disease?

Pronunciation: [mˌɒnə͡ʊd͡ʒˈɛnɪk dɪzˈiːz] (IPA)

A monogenic disease is a hereditary disorder caused by a mutation or abnormality in a single gene. There are various other terms used for monogenic diseases such as single-gene disorders, genetic diseases, Mendelian disorders, and inherited diseases. These terms are often used interchangeably to describe a condition that arises due to a mutation in a single gene. Some examples of monogenic diseases include cystic fibrosis, sickle cell anemia, and Huntington's disease. The treatment and management of these diseases depend on the specific genetic mutation and the associated symptoms. Genetic testing and counseling may also be recommended for individuals with a family history of monogenic diseases.

Synonyms for Monogenic disease:

What are the hypernyms for Monogenic disease?

A hypernym is a word with a broad meaning that encompasses more specific words called hyponyms.

What are the hyponyms for Monogenic disease?

Hyponyms are more specific words categorized under a broader term, known as a hypernym.

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