Terminology Service for NFDI4Health
All terms in HP
| Label | Id | Description |
|---|---|---|
| Cervical myelopathy | HP_0002318 | |
| Myelopathy | HP_0002196 | |
| Unsteady gait | HP_0002317 | |
| Gait disturbance | HP_0001288 | [The term gait disturbance can refer to any disruption of the ability to walk. In general, this can refer to neurological diseases but also fractures or other sources of pain that is triggered upon walking. However, in the current context gait disturbance refers to difficulty walking on the basis of a neurological or muscular disease.] |
| 1-methylhistidine | CHEBI_70958 | [A methylhistidine in which the methyl group is located at N-1.] |
| 1-methylhistidine zwitterion | CHEBI_133608 | [An alpha-amino acid zwitterion obtained by transfer of a proton from the carboxy to the amino group of 1-methylhistidine; major species at pH 7.3.] |
| human urinary metabolite | CHEBI_84087 | [Any metabolite (endogenous or exogenous) found in human urine samples.] |
| Metaphyseal sclerosis | HP_0004979 | [Abnormally increased density of metaphyseal bone.] |
| Abnormality of the metaphysis | HP_0000944 | [An abnormality of one or more metaphysis, i.e., of the somewhat wider portion of a long bone that is adjacent to the epiphyseal growth plate and grows during childhood.] |
| Hydranencephaly | HP_0002324 | [A defect of development of the brain characterized by replacement of greater portions of the cerebral hemispheres and the corpus striatum by cerebrospinal fluid (CSF) and glial tissue.] |
| Anencephaly | HP_0002323 | |
| obsolete Rudimentary to absent fibulae | HP_0004986 | |
| Thing | Thing | |
| early activation antigen CD69 (human) | PR_Q07108 | [A CD69 molecule that is encoded in the genome of human.] |
| CD69 molecule | PR_000001343 | [A protein that is a translation product of the human CD69 gene or a 1:1 ortholog thereof. A type II transmembrane protein with a C-type lectin binding domain in the extracellular portion of the molecule. Involved in lymphocyte proliferation and functions as a signal transmitting receptor in lymphocytes, natural killer (NK) cells, and platelets.] |
| CD69 (human) | gene_symbol_report | [A protein coding gene CD69 in human.] |
| Mesomelic leg shortening | HP_0004987 | [Shortening of the middle parts of the leg in relation to the upper and terminal segments.] |
| Mesomelia | HP_0003027 | [Shortening of the middle parts of the limbs (forearm and lower leg) in relation to the upper and terminal segments.] |
| Transient ischemic attack | HP_0002326 | |
| Stroke | HP_0001297 | [Sudden impairment of blood flow to a part of the brain due to occlusion or rupture of an artery to the brain.] |