Terminology Service for NFDI4Health
All terms in DOID
| Label | Id | Description |
|---|---|---|
| nasopharyngeal disease | DOID_9561 | |
| chronic pain | SYMP_0000837 | [Chronic pain is a pain that can range from mild to severe, and continues beyond the expected healing phase.] |
| dentin caries | DOID_10461 | |
| breakthrough pain | SYMP_0000838 | [Breakthrough pain is a pain that occurs with movement and is not controlled by a scheduled pain medication regimen, such that the pain breaks through the current regimen. This is usually referred to in the context of a short and long acting opioid, the short acting opioid being used to treat the breakthrough pain.] |
| hypoalgesia | SYMP_0000835 | [Hypoalgesia is a general symptom where there is a diminished sensitivity to painful stimulation.] |
| hyperalgesia | SYMP_0000836 | [Hyperalgesia is a general symptom where there is an increased response to a painful stimulus.] |
| visceral pain | SYMP_0000833 | [Visceral pain is a pain originated from organ tissues of the thorax, abdomen, or pelvis, It characterizes as deep, vague, difficult to locate pain that radiates away from the affected organ.] |
| nephrotic syndrome type 10 | DOID_0080386 | [A familial nephrotic syndrome characterized by early childhood onset that has_material_basis_in homozygous or compound heterozygous mutation in the EMP2 gene on chromosome 16p13.] |
| familial nephrotic syndrome | DOID_2590 | [A nephrotic syndrome that has_material_basis_in genetic mutations.] |
| hypoesthesia | SYMP_0000834 | [Hypoesthesia is a general symptom where there is a diminished sensitivity to stimulation.] |
| nephrotic syndrome type 12 | DOID_0080387 | [A familial nephrotic syndrome characterized by early childhood onset of steroid-resistant progressive renal failure with focal segmental glomerulosclerosis that has_material_basis_in homozygous or compound heterozygous mutation in the NUP93 gene on chromosome 16q13.] |
| nociceptive pain | SYMP_0000831 | [Nociceptive pain is a pain originated other than peripheral and central nervous system, caused by activation of nociceptive fibers.] |
| nephrotic syndrome type 7 | DOID_0080388 | [A familial nephrotic syndrome characterized by onset in the first decade of life of progressive renal disease with proteinuria and membranoproliferative glomerulonephritis that has_material_basis_in homozygous or compound heterozygous mutation in the DGKE gene on chromosome 17q22.] |
| neuropathic pain | SYMP_0000832 | [Neuropathic pain is a pain experienced by cancer patients caused by radiotherapy or chemotherapy damage to nerves, when cancer invades or compresses nerves, or when, during cancer treatment. This type of pain is typically described as burning, electrical, or strange feeling.] |
| nephrotic syndrome type 8 | DOID_0080389 | [A familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25.] |
| obsolete diabetes mellitus juvenile type, uncontrolled, with neurological manifestations | DOID_10469 | |
| chronic laryngitis | DOID_11797 | [A laryngitis in which symptoms last longer than three weeks. Gastroesophageal reflux, and lingering bronchitis can cause the disease.] |
| obsolete ovarian dermoid cyst with secondary melanocytic lesion | DOID_7590 | |
| gestational ovarian choriocarcinoma | DOID_7591 | [A choriocarcinoma of the ovary that develops in the presence of a preceding gestational event.] |
| acute pain | SYMP_0000839 | [Acute pain is a pain that is severe but lasts a relatively short time.] |