Terminology Service for NFDI4Health

Disease_Mapped_To_Gene

Go to external page http://purl.obolibrary.org/obo/NCIT_R176


A role used to assert a direct relationship between a disease, disorder or finding and a gene. This restriction can be used when a polymorphism or an abnormality in a gene is either a clinical marker for, a causative event for, or predisposes a subject to a disease. The domain and range for this role are 'Disease, Disorder or Finding' and 'Gene', respectively.

Synonyms: Disease_Mapped_To_Gene

Property info

Preferred Name

Disease_Mapped_To_Gene

Semantic Type

Conceptual Entity

code

R176

Property relations