All terms in DOID

Label Id Description
fallopian tube leiomyoma DOID_5124 [A fallopian tube benign neoplasm that has_material_basis_in smooth muscle cells.]
mediastinum leiomyoma DOID_5123 [A thoracic benign neoplasm that derives_from smooth muscle cells and is located_in the mediastinum.]
cerebellar liponeurocytoma DOID_6458 [A cerebellum cancer that is characterized by consistent neuronal, variable astrocytic and focal lipomatous differentiation.]
central nervous system leiomyoma DOID_5126 [A central nervous system benign neoplasm that derives_from smooth muscle cells.]
extrahepatic bile duct leiomyoma DOID_5125 [A gastrointestinal system benign neoplasm that derives_from smooth muscle cells and that is located_in the extrahepatic bile duct.]
rectal lipoma DOID_6459 [A rectal benign neoplasm that has_material_basis_in fat tissue.]
rectal benign neoplasm DOID_1984 [An intestinal benign neoplasm located_in the rectum.]
Nystagmus HP_0000639
Abnormal involuntary eye movements HP_0012547
breast osteosarcoma DOID_7787 [A breast sarcoma that arises from bone.]
deep leiomyoma DOID_5128 [A leiomyoma that is located_in deep soft tissue.]
adult spinal cord ependymoma DOID_7788
spinal cord ependymoma DOID_5503 [A high grade ependymoma that has_material_basis_in cells linking the spinal cord central canal.]
bizarre leiomyoma DOID_5127 [A leiomyoma that is characterized by large, atypical nuclei in otherwise normal appearing leiomyoma and rare or absent mitotic figures.]
intellectual developmental disorder with autistic features and language delay, with or without seizures DOID_0081430 [An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay, variable intellectual disability, impaired speech development, and behavioral abnormalities, most commonly on the autism spectrum and that has_material_basis_in heterozygous mutation in the TANC2 gene on chromosome 17q23.]
Abnormal scalp morphology HP_0001965
simple partial epilepsy DOID_5129
Abnormal glomerular mesangium morphology HP_0001966
Diffuse mesangial sclerosis HP_0001967
dimethylglycine dehydrogenase deficiency DOID_0081446 [An amino acid metabolic disorder that is characterized by a fish-like odor, chronic fatigue, and increased level of the muscle form of creatine kinase in serum and that has_material_basis_in homozygous mutation in the DMGDH on chromosome 5q14.]