| CFFA | cystic fibrosis factor activity |
|---|---|
| CFS | cancer family syndrome; Chiari-Frommel syndrome; chronic fatigue syndrome; craniofacial stenosis; cr... |
| CFTR | cystic fibrosis transmembrane conductance regulator |
| CHF | chick embryo fibroblast; chronic heart failure; congenital hepatic fibrosis; congestive heart failur... |
| COACH | cerebellar vermis hypoplasia/aplasia-oligophrenia-congenital ataxia-ocular colobomata-hepatic fibros... |
| skin diseases, vascular | Skin diseases affecting or involving the cutaneous blood vessels and generally manifested as inflammation, swelling, erythema, or necrosis in the affected area. (12 Dec 1998) |
|---|---|
| skin diseases, vesiculobullous | Skin diseases characterised by local or general distributions of blisters. They are classified according to the site and mode of blister formation. Lesions can appear spontaneously or be precipitated by infection, trauma, or sunlight. Aetiologies include immunologic and genetic factors. (12 Dec 1998) |
| skin diseases, viral | Skin diseases caused by viruses. (12 Dec 1998) |
| slow virus diseases | Diseases of viral origin, characterised by incubation periods of months to years, insidious onset of clinical manifestations, and protracted clinical course. Though the disease process is protracted, viral multiplication may not be unusually slow. Conventional viruses produce slow virus diseases such as subacute sclerosing panencephalitis, progressive multifocal leukoencephalopathy (leukoencephalopathy, progressive multifocal), and aids. Diseases produced by unconventional agents were originally considered part of this group. They are now called prion diseases. (12 Dec 1998) |
| social diseases | An obsolete term used to designate venereal disease's, especially gonorrhoea and syphilis. (05 Mar 2000) |
| nail diseases | Diseases of the nail plate and tissues surrounding it. The concept is limited to primates. (12 Dec 1998) |
| nasopharyngeal diseases | General or unspecified diseases of the nasopharynx. (12 Dec 1998) |
| neonatal diseases and abnormalities | Diseases existing at birth and often before birth, regardless of causation. Of these congenital diseases, those characterised by structural deformities are termed abnormalities. (12 Dec 1998) |
| stomatognathic diseases | General or unspecified diseases of the stomatognathic system, comprising the mouth, teeth, jaws, and pharynx. (12 Dec 1998) |
| neurodegenerative diseases | A varied assortment of central nervous system disorders characterised by gradual and progressive loss of neural tissue. (cecil textbook of medicine, 20th ed, p2050) (12 Dec 1998) |
| nose diseases | Disorders of the nose, general or unspecified. (12 Dec 1998) |
| nutritional and metabolic diseases | A collective term for nutritional disorders (result of poor assimilation or utilization of food) and metabolic disorders (result of poor metabolism or inherited enzyme abnormality). (12 Dec 1998) |
| deficiency diseases | A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (12 Dec 1998) |
| sweat gland diseases | Diseases of the sweat glands. (12 Dec 1998) |
| demyelinating diseases | Any condition characterised by the destruction of myelin and extensive loss of the myelin sheaths of the nerve fibres. It affects both the central and peripheral nervous systems. Its aetiology is at present unknown. (12 Dec 1998) |