Terminology Service < Semantic Lookup Platform

All individuals in MESHD

Label	Id	Description
Sinus Thrombosis, Intracranial	D012851	[Formation or presence of a blood clot (THROMBUS) in the CRANIAL SINUSES, large endothelium-lined venous channels situated within the SKULL. Intracranial sinuses, also called cranial venous sinuses, include the superior sagittal, cavernous, lateral, petrous sinuses, and many others. Cranial sinus thrombosis can lead to severe HEADACHE; SEIZURE; and other neurological defects.]
Sinusitis	D012852	[Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES.]
Sister Mary Joseph's Nodule	D058288	[Metastatic lesion of the UMBILICUS associated with intra-abdominal neoplasms especially of the GASTROINTESTINAL TRACT or OVARY.]
Situs Inversus	D012857	[A congenital abnormality in which organs in the THORAX and the ABDOMEN are opposite to their normal positions (situs solitus) due to lateral transposition. Normally the STOMACH and SPLEEN are on the left, LIVER on the right, the three-lobed right lung is on the right, and the two-lobed left lung on the left. Situs inversus has a familial pattern and has been associated with a number of genes related to microtubule-associated proteins.]
Sjogren's Syndrome	D012859	[Chronic inflammatory and autoimmune disease in which the salivary and lacrimal glands undergo progressive destruction by lymphocytes and plasma cells resulting in decreased production of saliva and tears. The primary form, often called sicca syndrome, involves both KERATOCONJUNCTIVITIS SICCA and XEROSTOMIA. The secondary form includes, in addition, the presence of a connective tissue disease, usually rheumatoid arthritis.]
Sjogren-Larsson Syndrome	D016111	[An autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS. It is caused by mutation of gene encoding microsomal fatty ALDEHYDE DEHYDROGENASE leading to defect in fatty alcohol metabolism.]
Skin Abnormalities	D012868	[Congenital structural abnormalities of the skin.]
Skin Diseases	D012871	[Diseases involving the DERMIS or EPIDERMIS.]
Skin Diseases, Bacterial	D017192	[Skin diseases caused by bacteria.]
Skin Diseases, Eczematous	D017443	[Any of a variety of eruptive skin disorders characterized by erythema, oozing, vesiculation, and scaling. Etiology is varied.]
Skin Diseases, Genetic	D012873	[Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.]
Skin Diseases, Infectious	D012874	[Skin diseases caused by bacteria, fungi, parasites, or viruses.]
Skin Diseases, Metabolic	D012875	[Diseases of the skin associated with underlying metabolic disorders.]
Skin Diseases, Papulosquamous	D017444	[A group of dermatoses with distinct morphologic features. The primary lesion is most commonly a papule, usually erythematous, with a variable degree of scaling on the surface. Plaques form through the coalescing of primary lesions.]
Skin Diseases, Parasitic	D012876	[Skin diseases caused by ARTHROPODS; HELMINTHS; or other parasites.]
Skin Diseases, Vascular	D017445	[Skin diseases affecting or involving the cutaneous blood vessels and generally manifested as inflammation, swelling, erythema, or necrosis in the affected area.]
Skin Diseases, Vesiculobullous	D012872	[Skin diseases characterized 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. Etiologies include immunologic and genetic factors. (From Scientific American Medicine, 1990)]
Skin Diseases, Viral	D017193	[Skin diseases caused by viruses.]
Skin Manifestations	D012877	[Dermatologic disorders attendant upon non-dermatologic disease or injury.]
Skin Neoplasms	D012878	[Tumors or cancer of the SKIN.]