Relation: has_mode_of_inheritance

translator_minimal

Relates a disease or phenotypic feature to its observed genetic segregation and assumed associated underlying DNA manifestation (i.e. autosomal, sex or mitochondrial chromosome).

URI: biolink:has_mode_of_inheritance

Domain and Range

DiseaseOrPhenotypicFeature -> _0..* GeneticInheritance

Parents

• is_a: has manifestation

Children

Used by

Other properties