All terms in BAO
| Label | Id | Description |
|---|---|---|
| Lewy body dementia | DOID_12217 | [A dementia and a synucleinopathy that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities.] |
| synucleinopathy | DOID_0050890 | [A neurodegenerative disease that is characterized by the abnormal accumulation of aggregates of alpha-synuclein protein in neurons, nerve fibres or glial cells.] |
| dementia | DOID_1307 | [A cognitive disorder resulting from a loss of brain function affecting memory, thinking, language, judgement and behavior.] |
| oligohydramnios | DOID_12215 | [A placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion.] |
| low tension glaucoma | DOID_13544 | |
| open-angle glaucoma | DOID_1067 | [A glaucoma characterized by optic nerve damage resulting in progressive loss of visual field and increased pressure in the eye due to trabecular blockage.] |
| hyperparathyroidism | DOID_13543 | [A parathyroid gland disease characterized by an overactivity of the parathyroid glands, leading to an excess of parathyroid hormone in the body.] |
| parathyroid gland disease | DOID_11201 | [An endocrine system disease that is located_in the parathyroid gland.] |
| peripheral nervous system neoplasm | DOID_1192 | [A nervous system cancer that is located_in the peripheral nervous system.] |
| water immersion lens | BAO_0150020 | |
| image acquisition device | BAO_0150021 | |
| protein-nucleotide interaction assay | BAO_0000394 | [Protein-nucleotide interaction] |
| complementary metal oxide semiconductor | BAO_0150024 | |
| area detector | BAO_0150022 | |
| electron multiplying charge coupled device | BAO_0150025 | |
| charge coupled device | BAO_0150023 | |
| photomultiplier tube | BAO_0150028 | |
| spot detector | BAO_0150026 | |
| photodiode | BAO_0150027 | |
| Larsen syndrome | DOID_14764 | [An autosomal dominant disease that is characterized by large-joint dislocations and characteristic craniofacial abnormalities.] |