Terminology Service for NFDI4Health
All terms in MESHD
| Label | Id | Description |
|---|---|---|
| Tick Toxicoses | D013986 | [Toxicoses caused by toxic substances secreted by the salivary glands of ticks; include tick paralysis (neurotropic toxin), sweating sickness (dermotropic toxin), and Rhipicephalus appendiculatus toxicosis (leukotropic toxin).] |
| Tick Paralysis | D013985 | [Paralysis caused by a neurotropic toxin secreted by the salivary glands of ticks.] |
| Tick Infestations | D013984 | [Infestations with soft-bodied (Argasidae) or hard-bodied (Ixodidae) ticks.] |
| Amputation, Traumatic | D000673 | [Loss of a limb or other bodily appendage by accidental injury.] |
| Self Mutilation | D012652 | [The act of injuring one's own body to the extent of cutting off or permanently destroying a limb or other essential part of a body.] |
| Xanthomatosis, Cerebrotendinous | D019294 | [An autosomal recessive lipid storage disorder due to mutation of the gene CYP27A1 encoding a CHOLESTANETRIOL 26-MONOOXYGENASE. It is characterized by large deposits of CHOLESTEROL and CHOLESTANOL in various tissues resulting in xanthomatous swelling of tendons, early CATARACT, and progressive neurological symptoms.] |
| Skull Base Neoplasms | D019292 | [Neoplasms of the base of the skull specifically, differentiated from neoplasms of unspecified sites or bones of the skull (SKULL NEOPLASMS).] |
| Nijmegen Breakage Syndrome | D049932 | [A chromosome instability syndrome resulting from a defective response to DNA double-strand breaks. In addition to characteristic FACIES and MICROCEPHALY, patients have a range of findings including RADIOSENSITIVITY, immunodeficiency, increased cancer risk, and growth retardation. Causative mutations occur in the NBS1 gene, located on human chromosome 8q21. NBS1 codes for nibrin, the key regulator protein of the R/M/N (RAD50/MRE11/NBS1) protein complex which senses and mediates cellular response to DNA DAMAGE caused by IONIZING RADIATION.] |
| Polyradiculoneuropathy, Chronic Inflammatory Demyelinating | D020277 | [A slowly progressive autoimmune demyelinating disease of peripheral nerves and nerve roots. Clinical manifestations include weakness and sensory loss in the extremities and enlargement of peripheral nerves. The course may be relapsing-remitting or demonstrate a step-wise progression. Protein is usually elevated in the spinal fluid and cranial nerves are typically spared. GUILLAIN-BARRE SYNDROME features a relatively rapid progression of disease which distinguishes it from this condition. (Adams et al., Principles of Neurology, 6th ed, p1337)] |
| Monteggia's Fracture | D009011 | [Fracture in the proximal half of the shaft of the ulna, with dislocation of the head of the radius.] |
| Septo-Optic Dysplasia | D025962 | [A condition resulting from congenital malformations involving the brain. The syndrome of septo-optic dysplasia combines hypoplasia or agenesis of the SEPTUM PELLUCIDUM and the OPTIC NERVE. The extent of the abnormalities can vary. Septo-optic dysplasia is often associated with abnormalities of the hypothalamic and other diencephalic structures, and HYPOPITUITARISM.] |
| Nicolau Syndrome | D065148 | [An uncommon complication of INTRAMUSCULAR INJECTION leading to variable degrees of necrosis of skin and underlying tissue.] |
| Alcohol Withdrawal Seizures | D020270 | [A condition where seizures occur in association with ethanol abuse (ALCOHOLISM) without other identifiable causes. Seizures usually occur within the first 6-48 hours after the cessation of alcohol intake, but may occur during periods of alcohol intoxication. Single generalized tonic-clonic motor seizures are the most common subtype, however, STATUS EPILEPTICUS may occur. (Adams et al., Principles of Neurology, 6th ed, p1174)] |
| Osteochondritis Dissecans | D010008 | [A type of osteochondritis in which articular cartilage and associated bone becomes partially or totally detached to form joint loose bodies. Affects mainly the knee, ankle, and elbow joints.] |
| Osteochondritis | D010007 | [Inflammation of a bone and its overlaying CARTILAGE.] |
| Osteoporotic Fractures | D058866 | [Breaks in bones resulting from low bone mass and microarchitectural deterioration characteristic of OSTEOPOROSIS.] |
| Osteoarthropathy, Primary Hypertrophic | D010004 | [A condition chiefly characterized by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, SEBORRHEA; HYPERHIDROSIS; periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. Inheritance is primarily autosomal recessive, but an autosomal dominant form exists.] |
| Osteoarthropathy, Secondary Hypertrophic | D010005 | [Symmetrical osteitis of the four limbs, chiefly localized to the phalanges and the terminal epiphyses of the long bones of the forearm and leg, sometimes extending to the proximal ends of the limbs and the flat bones, and accompanied by dorsal kyphosis and joint involvement. It is often secondary to chronic conditions of the lungs and heart. (Dorland, 27th ed)] |
| Osteitis Fibrosa Cystica | D010002 | [A fibrous degeneration, cyst formation, and the presence of fibrous nodules in bone, usually due to HYPERPARATHYROIDISM.] |
| Osteitis | D010000 | [Inflammation of the bone.] |