Terminology Service for NFDI4Health
All terms in BAO
| Label | Id | Description |
|---|---|---|
| glucocorticoid receptor import into nucleus | GO_0002147 | [The directed movement of a glucocorticoid receptor into the nucleus.] |
| steroid hormone receptor import into nucleus | GO_0002146 | [The directed movement of a steroid hormone receptor into the nucleus.] |
| thyroid crisis | DOID_12837 | |
| suppurative otitis media | DOID_11506 | [A otitis media which involves inflammation of the middle ear with infected effusion containing pus.] |
| Calu-1 cell | CLO_0002191 | |
| quadriplegia | DOID_12835 | |
| autonomic neuropathy | DOID_11504 | |
| photosensitive trichothiodystrophy | DOID_2960 | |
| aniseikonia | DOID_0050304 | |
| Cockayne syndrome | DOID_2962 | [An autosomal recessive disease that has material basis in rare mutations in two DNA excision repair proteins, ERCC-8 and ERCC-6, and characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging.] |
| EC 3.6.1.* (hydrolases acting on acid anhydrides in P-containing anhydrides) inhibitor | CHEBI_78927 | |
| survivin dimerisation modulator | CHEBI_78926 | |
| bursitis | DOID_2965 | |
| EC 3.6.1.3 (adenosinetriphosphatase) inhibitor | CHEBI_78928 | |
| Fasciola hepatica | NCBITaxon_6192 | |
| Chediak-Higashi syndrome | DOID_2935 | [An autosomal recessive disease characterized by oculocutaneous albinism, immune deficiency, coagulation deficiency and neuropathy; it is that has material basis in mutations in the CHS1 gene.] |
| LADD syndrome | DOID_0050331 | [An autosomal dominant disease that is characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes.] |
| enlarged vestibular aqueduct | DOID_0050332 | |
| fissured tongue | DOID_11514 | |
| Budd-Chiari syndrome | DOID_11512 |