ID Panel Indikationen 120614 - MedUni Wien: Startseite
O Alopecia Universalis Congenita (ALUNC) HR O Hereditary Hemorrhagic Telangiectasia ENG O Long/Short QT Syndrome, Autosomal Dominant AKAP9, KCNE1, KCNE2, KCNH2, KCNQ1, SCN4B, SNTA1, ANK2 O Tetralogy of Fallot NKX2-5 ... Retrieve Document
Atrichia with Papules ‘Alopecia Universalis’ AR (HR) Hereditary Angioedema (Quinke’s) AD (C1INH) C1 ESTERASE INHIBITOR Inhibits first component of complement Ataxia-Telangiectasia (Louis Bar) AR ATM PI3-kinase like domain Baere-Stevenson Syndrome (FGFr2) FGF RECEPTOR 2 ... Return Document
Ftp.cdc.gov
Drug-induced androgenic alopecia Lead-induced gout Drug-induced gout Crimean-Congo hemorrhagic fever Herpesviral [herpes simplex] infections Immunodeficiency following hereditary defective response to Epstein-Barr virus ... Return Document
Www.plosone.org
Alopecia universalis, 203655 (3) ; Atrichia with papular lesions, 209500 (3) Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome, 175050 (3) ; Pancreatic cancer (3) ; ENSG00000215693 Q8WYH8 Inhibitor of growth protein 5 (p28ING5) [Source: ... Retrieve Document
List Of Cutaneous Conditions - Wikipedia, The Free Encyclopedia
Marie–Unna hereditary hypotrichosis (Marie–Unna hypotrichosis) Spider telangiectasia, Spider nevus, Vascular spider) Spindle cell hemangioendothelioma Eosinophilic cutaneous conditions encompass a wide variety of diseases that are characterized histologically by the presence of ... Read Article
Www.nature.com
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT Endoglin (ENG) ALOPECIA UNIVERSALIS CONGENITA; ALUNC Hairless, mouse, homolog of (HR) 8p21.2 11A hair follicles without hair, Scalp, eyelashes, eyebrows, and body hair ... Retrieve Doc
Prevalence Of Rare Diseases: Bibliographic Data
X rare disease mean duration ; 701 Alopecia universalis 25 94058 Neovascular glaucoma 24.4 1199 Esophageal atresia 24.3 774 Hereditary hemorrhagic telangiectasia 16 137599 Stromal keratitis 16 2248 Hypoplastic left heart syndrome 15.1** ... Fetch Full Source
Ion AmpliSeq™ Inherited Disease Panel Target Gene List
Ion AmpliSeq ™ Inherited Disease Panel target gene list Symbol Disease ENG Hereditary Hemorrhagic Telangiectasia EXT1 Exostoses, Multiple, Type 1 HR Alopecia Universalis Congenita (ALUNC) IDS Hunter Syndrome (MPSII) IDUA Hurler Syndrome ... Access Full Source
Www.nature.com
Alopecia universalis, 203655 (3); Atrichia with papular lesions, 209500 (3) 8p21.1 ESCO2 Establishment of cohesion 1, S. cerevisiae, homolog of, 2 Roberts syndrome, 268300 (3) Hereditary hemorrhagic telangiectasia-1, 187300 (3) LMX1B, NPS1 ... Read Document
Genetic Disorders In Arab Populations Indexed In The CTGA ...
187300 Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber A B 187400 Testicular Torsion B Sa 187500 Tetralogy of Fallot B Le Li Ma O U 187600 Thanatophoric Dysplasia, Type I Mo O U 203655 Alopecia Universalis Congenita O ... Return Doc
Auftrag Zur DNA Diagnostik - MedUni Wien: Startseite
O Alopecia Universalis Congenita (ALUNC) HR O Darier Disease ATP2A2 O Dyskeratosis O Hereditary Hemorrhagic Telangiectasia ENG O Long/Short QT Syndrome, Autosomal Dominant AKAP9, KCNE1, KCNE2, KCNH2, KCNQ1, SCN4B, SNTA1, ANK2 O ... Retrieve Full Source
INDEX [books.mcgraw-hill.com]
Alopecia. nonscarring, 928Ð940. alopecia areata, 928Ð930, 929f, 931f. alopecia totalis, 928. alopecia universalis, 928, 931f. anagen effluvium, 940, 940f. androgenetic alopecia, 932Ð936, 933f, 935fÐ936f. neoplastica, 482. telogen effluvium, 937Ð939, 938tÐ939t, 939f. ... Retrieve Content
ISSN: 0001-7310 ACTAS Dermo-Sifiliográficas
Prostatic hyperplasia, and alopecia areata universalis who was receiving treatment with atenolol, atorvastatin, allopurinol, rosacea, unilateral nevoid telangiectasia, hereditary hemorrhagic telangiectasia, benign hereditary telangiectasia, many genodermatoses, ... Fetch Content
Www.barabasilab.com
Alopecia_universalis [704.09] OTHER ALOPECIA 86 Alpers_syndrome [330.8] Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome Disease of capillaries 834 Kala-azar [085] LEISHMANIASIS VISCERAL (KALA-AZAR) 835 Kallikrein,_decreased_urinary_activity_of ... Get Content Here
The Human Disease Network - CCNR
Alopecia universalis Alpers syndrome 87 Alpha-actinin-3 deficiency 92 Alport syndrome Amelogenesis imperfecta Analbuminemia 107 Anderson 833 Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome 830 Jervell and Lange-Nielsen syndrome 809 Infundibular hypoplasia and hypopituitarism ... Return Document
PNAS - University Of Notre Dame
Alopecia universalis Alpers syndrome 87 Alpha-actinin-3 deficiency 92 Alport syndrome Amelogenesis imperfecta Analbuminemia 107 Anderson 833 Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome 830 Jervell and Lange-Nielsen syndrome 809 Infundibular hypoplasia and hypopituitarism ... Return Document
Www.hrsa.gov
For the control and prevention of hemorrhagic episodes and for surgical prophylaxis in patients with hemophilia A For the treatment of patients with hereditary antithrombin III deficiency in connection with surgical or obstetrical procedures or when they suffer from thromboembolism. ... Retrieve Doc
Stasis Dermatitis - Wikipedia, The Free Encyclopedia
Hereditary hemorrhagic telangiectasia; Vascular nevus. Cherry hemangioma; Halo nevus; Spider angioma; Veins: Inflammation. Phlebitis; Venous thrombosis / Thrombophlebitis. primarily lower limb. Deep vein thrombosis; abdomen. Hepatic veno-occlusive disease; Budd–Chiari syndrome; ... Read Article
For the control and prevention of hemorrhagic episodes and for surgical prophylaxis in patients with hemophilia A For the treatment of patients with hereditary antithrombin III deficiency in connection with surgical or obstetrical procedures or when they suffer from thromboembolism. ... Read More
Bioinformatics.oxfordjournals.org
Sheet3 Sheet2 Diseases Tuberculosis UNSPECIFIED PULMONARY TUBERCULOSIS CONFIRMATION UN Listeria_monocytogenes Other zoonotic bacterial diseases Leprosy ... Read Full Source
List Of Diseases (A) - Wikipedia, The Free Encyclopedia
Albright's hereditary osteodystrophy; Albright's syndrome; Alcaptonuria; Alopecia universalis; Alopecia, epilepsy, pyorrhea, mental subnormality; Alp–Alz Edit. Alpers disease; Argentine hemorrhagic fever; Arginase deficiency; Arginemia; ... Read Article
Cutaneous Collagenous Vasculopathy: A Rare Cutaneous ...
UE, and trunk HTN, HPL, hyperuricemia, BPH, alopecia universalis 9Lloyd2 2011 16 F LE, UE, and trunk Mood disorder 10 Current report 2011 59 M LE →abdomen DM, HTN, HPL, capillary venules in the telangiectasias of hereditary hemorrhagic telangiectasia and generalized essential ... Retrieve Full Source
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