Terminology Service for NFDI4Health
All terms in MESHD
| Label | Id | Description |
|---|---|---|
| Heart Neoplasms | D006338 | [Tumors in any part of the heart. They include primary cardiac tumors and metastatic tumors to the heart. Their interference with normal cardiac functions can cause a wide variety of symptoms including HEART FAILURE; CARDIAC ARRHYTHMIAS; or EMBOLISM.] |
| Myxoma | D009232 | [A benign neoplasm derived from connective tissue, consisting chiefly of polyhedral and stellate cells that are loosely embedded in a soft mucoid matrix, thereby resembling primitive mesenchymal tissue. It occurs frequently intramuscularly where it may be mistaken for a sarcoma. It appears also in the jaws and the skin. (From Stedman, 25th ed)] |
| Vitamin K Deficiency Bleeding | D006475 | [Neonatal nasogastric or intracranial hemorrhage caused by vitamin K deficiency., Hemorrhage caused by vitamin K deficiency.] |
| Vitamin K Deficiency | D014813 | [A nutritional condition produced by a deficiency of VITAMIN K in the diet, characterized by an increased tendency to hemorrhage (HEMORRHAGIC DISORDERS). Such bleeding episodes may be particularly severe in newborn infants. (From Cecil Textbook of Medicine, 19th ed, p1182)] |
| Infant Nutrition Disorders | D007228 | [Disorders caused by nutritional imbalance, either overnutrition or undernutrition, occurring in infants ages 1 month to 24 months., Malnutrition, occurring in infants ages 1 month to 24 months, which is due to insufficient intake of food, dietary nutrients, or a pathophysiologic condition which prevents the absorption and utilization of food. Growth and development are markedly affected.] |
| Prolidase Deficiency | D056732 | [Rare autosomal recessive disorder of metabolism due to mutations in the prolidase gene. It is characterized by recurrent lower extremity skin ulcers, recurrent infections, and FACIES, often with INTELLECTUAL DISABILITY.] |
| Nevus | D009506 | [A circumscribed stable malformation of the skin and occasionally of the oral mucosa, which is not due to external causes and therefore presumed to be of hereditary origin.] |
| Nevi and Melanomas | D018326 | [A collective term for the various types of nevi and melanomas.] |
| Autoimmune Lymphoproliferative Syndrome | D056735 | [Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY., Autoimmune lymphoproliferative syndrome due to mutations in CASPASE 8 gene.] |
| Monilethrix | D056734 | [Rare autosomal dominant disorder of the hair shaft. The clinical features of the disease include HYPOTRICHOSIS, dry, and/or brittle hair, with varying degrees of ALOPECIA. Mutations in the hair-specific keratin genes KRTHB1, KRTHB3, or KRTHB6 are associated with monilethrix. Autosomal recessive monilethrix with limited HYPOTRICHOSIS are also known. Mutations in Dsg4, Liph, and P2ry5 protein genes are associated with the recessive form of monilethrix.] |
| Hemorrhagic Fever, American | D006478 | [Diseases caused by American hemorrhagic fever viruses (ARENAVIRUSES, NEW WORLD).] |
| Hemorrhagic Fever, Crimean | D006479 | [A severe, often fatal disease in humans caused by the Crimean-Congo hemorrhagic fever virus (HEMORRHAGIC FEVER VIRUS, CRIMEAN-CONGO).] |
| Facial Dermatoses | D005148 | [Skin diseases involving the FACE.] |
| Sinus Pericranii | D020779 | [Rare vascular anomaly involving a communication between the intracranial and extracranial venous circulation via diploe, the central spongy layer of cranial bone. It is often characterized by dilated venous structures on the scalp due to abnormal drainage from the intracranial venous sinuses. Sinus pericranii can be congenital or traumatic in origin.] |
| Central Nervous System Vascular Malformations | D020785 | [Congenital, inherited, or acquired abnormalities involving ARTERIES; VEINS; or venous sinuses in the BRAIN; SPINAL CORD; and MENINGES.] |
| Soft Tissue Infections | D018461 | [Infections of non-skeletal tissue, i.e., exclusive of bone, ligaments, cartilage, and fibrous tissue. The concept is usually referred to as skin and soft tissue infections and usually subcutaneous and muscle tissue are involved. The predisposing factors in anaerobic infections are trauma, ischemia, and surgery. The organisms often derive from the fecal or oral flora, particularly in wounds associated with intestinal surgery, decubitus ulcer, and human bites. (From Cecil Textbook of Medicine, 19th ed, p1688)] |
| Nevus of Ota | D009507 | [A macular lesion on the side of the FACE, involving the CONJUNCTIVA and EYELIDS, as well as the adjacent facial skin, SCLERA; OCULOMOTOR MUSCLES; and PERIOSTEUM. Histological features vary from those of a MONGOLIAN SPOT to those of a BLUE NEVUS.] |
| Nevus, Pigmented | D009508 | [A nevus containing melanin. The term is usually restricted to nevocytic nevi (round or oval collections of melanin-containing nevus cells occurring at the dermoepidermal junction of the skin or in the dermis proper) or moles, but may be applied to other pigmented nevi.] |
| Fractures, Comminuted | D018460 | [A fracture in which the bone is splintered or crushed into a number of pieces.] |
| Toothache | D014098 | [Pain in the adjacent areas of the teeth.] |