| HSE | herpes simplex encephalitis; hemorrhagic shock and encephalopathy |
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| HSG | herpex simplex genitalis; hysterosalpingogram, hysterosalpingography |
| HSK | herpes simplex keratitis |
| HSL | herpes simplex labialis; hormone-sensitive lipase |
| HSV | herpes simplex virus; high selective vagotomy; hop stunt viroid; hyperviscosity syndrome |
| herpes simplex virus 1 helicase-primase | <enzyme> Complex of three herpes-encoded gene products (ul52, ul5, and ul8) in addition to helicase activity, contains a tightly associated complex that may prime lagging strand synthesis as it unwinds DNA at the viral replication fork Registry number: EC 3.1.- Synonym: hsv-1 helicase-primase, ul5 protein, hsv helicase-primase complex, ul52 protein, ul8 protein (26 Jun 1999) |
|---|---|
| herpes simplex virus DNA polymerase | <enzyme> 3'-5'-exonuclease activity is associated with herpes simplex virus DNA polymerase; interacts with hsv-1 ul42 protein Registry number: EC 3.1.11.- Synonym: hsv DNA polymerase, polymerase associated exonuclease, herpes simplex virus 1 ul30 polymerase, hsv-1 ul30 protein, DNA polymerase ul30, hsv-1 (26 Jun 1999) |
| herpes simplex virus protein vmw65 | Trans-acting protein that combines with host factors to induce immediate early gene transcription in herpes simplex virus. (12 Dec 1998) |
| herpes simplex virus type 1 UL13 protein kinase | <enzyme> Phosphorylates icp22 and involved in the accumulation of alpha and gamma mrnas and proteins in the infected cells; aa sequence has been determined Registry number: EC 2.7.1.- Synonym: ul13 protein kinase, hsv-1, hsv-1 ul13 protein, hsv-1 ul13 pk, u(l)13 protein kinase, protein kinase ul13 (26 Jun 1999) |
| prurigo simplex | A mild form of prurigo having a pronounced tendency to relapse. (05 Mar 2000) |
| xanthoma tuberosum simplex | Xanthomatosis associated with familial type II, and occasionally type III, hyperlipoproteinaemia. Synonym: xanthoma tuberosum simplex. (05 Mar 2000) |
| dermatitis simplex | Blushing or redness of the skin caused by a toxic reaction or a neurovascular phenomenon. Synonym: dermatitis simplex. (05 Mar 2000) |
| ichthyosis simplex | most common form of ichthyosis characterised by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait. (12 Dec 1998) |
| epidermolysis bullosa simplex | This represents a group of rare inherited disorders in which blistering of the skin occurs in response to skin trauma. Large fluid-filled blisters can occur in response to injury, skin rubbing, chafing or even increases in room temperature. Secondary bacterial infection of the blisters is common. Complications include oesophageal stricture, infections, loss of function of hands and feet and malnutrition. The dermatologist is the expert in the evaluation and treatment of this disorder. (27 Sep 1997) |
| erythema simplex | Blushing or redness of the skin caused by a toxic reaction or a neurovascular phenomenon. Synonym: dermatitis simplex. (05 Mar 2000) |
| lichen simplex chronicus | A thickened area of itching skin resulting from rubbing and scratching. (05 Mar 2000) |
| lobulus simplex | The smaller anterior part of the posterior lobe of the cerebellum, demarcated by the primary fissure from the anterior lobe rostrally and from the large caudal subdivision of the posterior lobe caudally. Synonym: lobulus simplex. (05 Mar 2000) |
| lymphangioma simplex | A circumscribed region or focus of several to numerous lymphatic vessels that are moderately dilated. Synonym: simple lymphangiectasis. (05 Mar 2000) |
| lymphangioma superficium simplex | A congenital nevoid lesion consisting of a circumscribed group of tense lymph vesicles. Synonym: lupus lymphaticus, lymphangiectodes, lymphangioma capillare varicosum, lymphangioma superficium simplex. (05 Mar 2000) |
| acute vascular purpura | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |