WormMine

WS296

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0080578 digenic disease Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A polygenic disease that is characterized by expression of a phenotype that requires the presence of pathogenic variants in two different genes.

1 Ontology

Name
Disease Ontology

4 Parents

Identifier Name Description
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:630 genetic disease A disease that has_material_basis_in genetic variations in the human genome.
DOID:0080578 digenic disease A polygenic disease that is characterized by expression of a phenotype that requires the presence of pathogenic variants in two different genes.
DOID:0080577 polygenic disease A genetic disease that is characterized by the additive contributions of variants in multiple genes at different loci.

50 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0080578 DOID:0050553
is_a DOID:0080578 DOID:0050715
is_a DOID:0080578 DOID:0050947
is_a DOID:0080578 DOID:0050967
is_a DOID:0080578 DOID:0060369
is_a DOID:0080578 DOID:0060912
is_a DOID:0080578 DOID:0060916
is_a DOID:0080578 DOID:0060917
is_a DOID:0080578 DOID:0060918
is_a DOID:0080578 DOID:0060984
is_a DOID:0080578 DOID:0070014
is_a DOID:0080578 DOID:0070015
is_a DOID:0080578 DOID:0070016
is_a DOID:0080578 DOID:0070017
is_a DOID:0080578 DOID:0070018
is_a DOID:0080578 DOID:0070019
is_a DOID:0080578 DOID:0070020
is_a DOID:0080578 DOID:0070021
is_a DOID:0080578 DOID:0070022
is_a DOID:0080578 DOID:0070023
is_a DOID:0080578 DOID:0070024
is_a DOID:0080578 DOID:0070025
is_a DOID:0080578 DOID:0070026
is_a DOID:0080578 DOID:0070095
is_a DOID:0080577 DOID:0080578
is_a DOID:4 DOID:0080578
is_a DOID:630 DOID:0080578
is_a DOID:0080578 DOID:0080952
is_a DOID:0080578 DOID:0090100
is_a DOID:0080578 DOID:0110090

0 Synonyms