Terminology Service for NFDI4Health
All terms in DOID
| Label | Id | Description |
|---|---|---|
| Human orthopneumovirus | NCBITaxon_11250 | |
| Orthopneumovirus | NCBITaxon_1868215 | |
| tubular aggregate myopathy | DOID_0080089 | |
| obsolete Rotator cuff shoulder syndrome and allied disorder | DOID_12702 | |
| hyperprolactinemia | DOID_12700 | [An acquired metabolic disease that has_material_basis_in the presence of abnormally-high levels of prolactin in the blood.] |
| acquired metabolic disease | DOID_0060158 | [A disease of metabolism that has _material_basis_in enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to an endocrine organ disease, organ malfunction, inadequate intake, dietary deficiency, or malabsorption.] |
| Pneumoviridae | NCBITaxon_11244 | |
| nonsyndromic congenital nail disorder 2 | DOID_0080080 | |
| myoclonic cerebellar dyssynergia | DOID_12707 | |
| Friedreich ataxia | DOID_12705 | |
| ataxia telangiectasia | DOID_12704 | |
| nonsyndromic congenital nail disorder 7 | DOID_0080085 | |
| nonsyndromic congenital nail disorder 8 | DOID_0080086 | |
| nonsyndromic congenital nail disorder 9 | DOID_0080087 | |
| nonsyndromic congenital nail disorder 10 | DOID_0080088 | |
| nonsyndromic congenital nail disorder 3 | DOID_0080081 | |
| nonsyndromic congenital nail disorder 4 | DOID_0080082 | [A nail disease that is characterized by absence of fingernails and toenails, has_material_basis_in homozygous or compound heterozygous mutation in the R-spondin-4 gene on chromosome 20p13.] |
| nonsyndromic congenital nail disorder 5 | DOID_0080083 | |
| nonsyndromic congenital nail disorder 6 | DOID_0080084 | |
| obsolete medullary sponge kidney | DOID_12713 |