'disease or disorder' susceptibility, 'gene' form
|
susceptibility_by_gene.yaml |
[A susceptibility or predisposition to 'disease or disorder' in which the cause of the disease is a mutation in the 'gene' gene.] |
'disease or disorder' susceptibility
|
inherited_susceptibility.yaml |
[An inherited susceptibility or predisposition to developing 'disease or disorder'.] |
iatrogenic 'disease'
|
iatrogenic.yaml |
[A 'disease' that has an iatrogenic cause.] |
'multicellular anatomical structure' adenosquamous carcinoma
|
adenosquamous_carcinoma.yaml |
[Any carcinoma that that involves the 'multicellular anatomical structure' and is characterized by the presence of glandular and squamous malignant epithelial components.] |
MONDO_0006074
|
MONDO_0006074 |
|
owl_thing carcinoma in situ
|
carcinoma_in_situ.yaml |
[A carcinoma in situ involving a owl_thing.] |
MONDO_0004647
|
MONDO_0004647 |
|
MONDO_0004993
|
MONDO_0004993 |
|
allergic 'disease'
|
allergic_form_of_disease.yaml |
[A 'disease' with a basis in a pathological type I hypersensitivity reaction.] |
'anatomical entity' lesion
|
lesioned.yaml |
[Lesioned form of 'anatomical entity'.] |
hemangioma of 'anatomical entity'
|
hemangioma.yaml |
[A hemangioma that involves the 'anatomical entity'.] |
MONDO_0006500
|
MONDO_0006500 |
|
'owl_thing' 'disease'
|
specific_disease_by_dysfunctional_structure.yaml |
[Any 'disease' in which the causes of the disease is a perturbation of the 'owl_thing' leading to its dysfunction.] |
MONDO_0024491
|
MONDO_0024491 |
|
MONDO_0005058
|
MONDO_0005058 |
|
MONDO_0020573
|
MONDO_0020573 |
|
owl_thing rhabdomyosarcoma
|
rhabdomyosarcoma.yaml |
[A malignant mesenchymal tumor with skeletal muscle differentiation affecting the owl_thing.] |
MONDO_0045036
|
MONDO_0045036 |
|
MONDO_0005062
|
MONDO_0005062 |
|
SO_0000704
|
SO_0000704 |
|