Mendelian trait
Term · Chemistry · MLC-T-CHM-007176
A phenotype whose inheritance follows Mendel's laws, being governed by a single gene locus with dominant or recessive expression, so that it appears in predictable ratios among relatives. Cystic fibrosis, an autosomal recessive condition, and Huntington disease, an autosomal dominant one, are examples. Polygenic traits such as height contrast with them by varying continuously across a population.
| Identifier | MLC-T-CHM-007176 |
|---|---|
| Field | Chemistry |
| Subject | Chemistry and Human Health |
| References | PAC, 2016, 88, 713. 'Glossary of terms used in developmental and reproductive toxicology (IUPAC Recommendations 2016)' on page 777 (https://doi.org/10.1515/pac-2015-1202) |
| See also | Mendelian inheritance |
Record as JSON
{
"id": "MLC-T-CHM-007176",
"term": "Mendelian trait",
"field": "Chemistry",
"definition": "A phenotype whose inheritance follows Mendel's laws, being governed by a single gene locus with dominant or recessive expression, so that it appears in predictable ratios among relatives. Cystic fibrosis, an autosomal recessive condition, and Huntington disease, an autosomal dominant one, are examples. Polygenic traits such as height contrast with them by varying continuously across a population.",
"subject": "Chemistry and Human Health",
"see_also": [
"Mendelian inheritance"
],
"references": [
"PAC, 2016, 88, 713. 'Glossary of terms used in developmental and reproductive toxicology (IUPAC Recommendations 2016)' on page 777 (https://doi.org/10.1515/pac-2015-1202)"
],
"url": "https://mlchart.com/terminology/chemistry/mendelian-trait/"
}
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