|
hereditary 'disease'
|
hereditary.yaml |
[An instance of 'disease' that is caused by an inherited genomic modification in an individual.] |
|
CL_0000000
|
CL_0000000 |
|
|
'disease' of 'anatomical entity' or 'cell'
|
location.yaml |
[A 'disease' that involves the 'anatomical entity' or 'cell'.] |
|
HP_0003621
|
HP_0003621 |
|
|
CHEBI_24431
|
CHEBI_24431 |
|
|
GO_0016068
|
GO_0016068 |
|
|
MONDO_0700005
|
MONDO_0700005 |
|
|
GO_0098687
|
GO_0098687 |
|
|
'chromosome' disorder
|
chromosome_type.yaml |
[A chromosomal disorder in which 'chromosome' is affected.] |
|
mild 'disease'
|
mild.yaml |
[An instance of 'disease' in which the disease presentation is mild in severity.] |
|
owl_thing adenocarcinoma
|
adenocarcinoma.yaml |
[A carcinoma that arises from glandular epithelial cells of the owl_thing] |
|
MONDO_0004970
|
MONDO_0004970 |
|
|
HP_0000118
|
HP_0000118 |
|
|
benign owl_thing neoplasm
|
benign_neoplasm.yaml |
[A benign neoplasm involving a owl_thing.] |
|
MONDO_0005165
|
MONDO_0005165 |
|
|
HP_0000005
|
HP_0000005 |
|
|
HP_0000006
|
HP_0000006 |
|
|
disease_has_major_feature.yaml
|
disease_has_major_feature.yaml |
|
|
inflammation of 'anatomical structure'
|
inflammatory_disease_by_site.yaml |
[An inflammatory disease involving a pathogenic inflammatory response in the 'anatomical structure'.] |
|
'material entity' abuse
|
substance_abuse.yaml |
[The abuse or overuse of 'material entity'.] |
