|
limb nerve
|
UBERON_0003440 |
|
|
duodenum
|
UBERON_0002114 |
|
|
peliosis hepatis
|
DOID_914 |
|
|
jejunum
|
UBERON_0002115 |
|
|
atrophic muscular disease
|
DOID_913 |
[A neuromuscular disease that is characterized by an abnormal reduction in the muscle volume and atrophy.] |
|
ileum
|
UBERON_0002116 |
|
|
gallbladder
|
UBERON_0002110 |
|
|
liver inflammatory pseudotumor
|
DOID_918 |
|
|
liver leiomyoma
|
DOID_917 |
|
|
kidney
|
UBERON_0002113 |
|
|
liver
|
UBERON_0002107 |
|
|
occipital lobe neoplasm
|
DOID_910 |
|
|
small intestine
|
UBERON_0002108 |
|
|
Clostridia
|
NCBITaxon_186801 |
|
|
gastrointestinal lymphoma
|
DOID_903 |
|
|
obsolete malignant non-epithelial hepatic and intrahepatic bile duct neoplasm
|
DOID_902 |
|
|
liver lymphoma
|
DOID_901 |
|
|
hepatopulmonary syndrome
|
DOID_900 |
|
|
liver fibroma
|
DOID_907 |
|
|
osteogenesis imperfecta type 4
|
DOID_0110340 |
[An osteogenesis imperfecta that is characterized by bone fragility and normal sclerae and has_material_basis_in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.] |
