ONKI3 | Medical Subject Headings

1. Val av ontologi/vokabulär

Med hjälp av ONKI-bläddraren kan du lätt bekanta dig med olika ontologier och vokabulärer. Du kan välja att använda någon av dessa genom att integrera din applikation i ONKI-servicen eller så kan du alternativt ladda innehållet i en ontologi/vokabulär via ONKI-bläddraren och använda det i din applikation på det sätt som ontologins/vokabulärens användarvillkor tillåter.

Du kan också skapa en egen ontologi/vokabulär och ladda in den i ONKI-servicen. En ontologi/vokabulär som du vill ladda in kan du antingen skapa från början eller så kan du bearbeta en ontologi/vokabulär som redan finns i ONKI. Som format för en ontologi/vokabulär som ska laddas in i ONKI kan du använda antingen SKOS- eller OWL-formatet. Tjänstens upprätthållare rekommenderar SKOS-formatet som framställningssätt för ordlistor och klassificeringar, medan det för mera omfattande ontologier torde vara bäst att använda OWL-språket. Ontologi/vokabulär -filen kan du hämta till ONKI-servicen via laddnings. När du har fyllt i formuläret publiceras din ontologi/vokabulär i ONKI-servicen inom några vardagar.

2. Användning av ONKI-servicen vid informationssökning och innehållsbeskrivning

Användning av ONKI-servicen vid informationssökning och/eller innehållsbeskrivning är gratis men kräver registrering. De uppgifter som ombeds vid registreringen används för att få en helhetsbild av vilka tjänster och hur mycket dessa tjänster används och av vem. Vi kan också utnyttja e-postadresserna för att informera stadigvarande användare om viktiga förändringar i anslutning till tjänsten.

ONKI-väljaren

I formuläret som du gör för informationssökning och innehållsbeskrivning kan ONKI-bläddraren användas som ett intelligent textbox-fält. När användaren skriver text i fältet erbjuder ONKI-systemet färdiga alternativ under fältet. Alternativens avgränsning baserar sig på de valbara begreppens stavning och de kan begränsas med hjälp av jokertecken i ONKI-systemet. Alternativen hämtas ur ontologierna/vokabulärerna som är publicerade i ONKI-systemet, beroende på de användarinställningar som du definierat i formuläret.

Vid innehållsbeskrivning kan du vara inriktad på valet av ett begrepp (t.ex. en typ av museiföremål: yxor), men vid informationssökning kan du använda utvidgad sökning med ontologins relationsinformation. Till exempel när man väljer sökordet verktyg som sökvillkor i museiföremålens sökformulär så kan man automatiskt lägga till bl.a. följande söktermer: yxor, cirklar, mejslar, o.s.v.

Maskinella gränssnitt

Via maskinella gränssnitt (Web service och HTTP) kan du utnyttja ONKI mer flexibelt. Behov av flexibilitet fanns bl.a. i SAHA metadata-editorn som utvecklades i SeCo och vid genomförandet kom man fram till att utnyttja gränssnittet för ONKIs web service. Via Web service-gränssnittet kan du ta reda på bl.a. namn som motsvarar begreppens URI på olika språk. Du kan bekanta dig med användning av gränssnittet via testsidan.

Ontologiservicen ONKI är en nationell tjänst som skapats av forskningsgruppen för semantisk beräkning (SeCo) som fungerar vid Aalto-universitetets högskola för teknikvetenskaper och Helsingfors universitet. Tjänsten har utvecklats inom ramen för projekten FinnONTO och FinnONTO 2.0. För utvecklandet av ONKI ansvarar SeCo:s ONKI-arbetsgrupp, till vilken hör:

Jouni Tuominen, doktorand
Eero Hyvönen, professor

Tidigare medlemmar: Kim Viljanen, Rami Alatalo

Tilläggsuppgifter om ONKI

suomeksi på svenska in English

Visningssätt för begreppens/termernas förhållanden: under varandra bredvid varandra

Det sätt begreppsrelationer visas: separat i hierarkin

Wiskott-Aldrichs syndrom

Laddar resultat...


Hierarki:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Purpura ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Platelet Disorders ∟ Thrombocytopenia ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Immunologic Deficiency Syndromes ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Skin Manifestations ∟ Purpura ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Manifestations ∟ Purpura ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom 54 sidobegrepp ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ von Willebrand Disease \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic \| ∟ Agammaglobulinemia \| ∟ Ataxia Telangiectasia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Severe Combined Immunodeficiency X
Bredare villkor:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Wiskott-Aldrichs syndrom Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Wiskott-Aldrichs syndrom Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Wiskott-Aldrichs syndrom Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Purpura ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Platelet Disorders ∟ Thrombocytopenia ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Wiskott-Aldrichs syndrom Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Immunologic Deficiency Syndromes ∟ Wiskott-Aldrichs syndrom Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Skin Manifestations ∟ Purpura ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Manifestations ∟ Purpura ∟ Purpura, Thrombocytopenic ∟ Wiskott-Aldrichs syndrom Blood Coagulation Disorders, Inherited > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Genetic Diseases, X-Linked > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Blood Coagulation Disorders, Inherited > Blood Coagulation Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Purpura, Thrombocytopenic > Purpura > Blood Coagulation Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Purpura, Thrombocytopenic > Blood Coagulation Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Purpura, Thrombocytopenic > Thrombocytopenia > Blood Platelet Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Hemorrhagic Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Immunologic Deficiency Syndromes > Immune System Diseases > Medical Subject Headings (MeSH) Purpura, Thrombocytopenic > Immune System Diseases > Medical Subject Headings (MeSH) Purpura, Thrombocytopenic > Purpura > Skin Manifestations > Signs and Symptoms > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) Purpura, Thrombocytopenic > Purpura > Skin Manifestations > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Anmärkning:	A rare, X-linked immunodeficiency syndrome characterized by eczema, thrombocytopenic purpura, and recurrent pyogenic infection. It is seen exclusively in young boys. Typically, IMMUNOGLOBULIN M levels are low and IMMUNOGLOBULIN A and IMMUNOGLOBULIN E levels are elevated. Lymphoreticular malignancies are common. X
historyNote*:	85; was ALDRICH SYNDROME 1963-84 X
onlineNote*:	use WISKOTT-ALDRICH SYNDROME to search ALDRICH SYNDROME 1966-84 X
publicMeSHNote*:	85; was ALDRICH SYNDROME 1963-84 X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	NLMX
Typ:	Concept X
Samordna villkor:	Afibrinogenemia \| Bernard-Soulier Syndrome \| Disseminated Intravascular Coagulation \| Factor V Deficiency \| Factor VII Deficiency \| Factor X Deficiency \| Factor XI Deficiency \| Factor XII Deficiency \| Factor XIII Deficiency \| Hemophilia A \| Hemophilia B \| Hypoprothrombinemias \| Platelet Storage Pool Deficiency \| Purpura, Thrombocytopenic, Idiopathic \| Thrombasthenia \| Thrombocythemia, Hemorrhagic \| Vascular Hemostatic Disorders \| Vitamin K Deficiency \| von Willebrand Disease \| Waterhouse-Friderichsen Syndrome \| Androgen-Insensitivity Syndrome \| Choroideremia \| Dyskeratosis Congenita \| Ectodermal Dysplasia 1, Anhidrotic \| Fabry Disease \| Focal Dermal Hypoplasia \| Glycogen Storage Disease Type IIb \| Glycogen Storage Disease Type VIII \| Granulomatous Disease, Chronic \| Hyper-IgM Immunodeficiency Syndrome, Type 1 \| Hypophosphatemic Rickets, X-Linked Dominant \| Ichthyosis, X-Linked \| Mental Retardation, X-Linked \| Muscular Dystrophy, Duchenne \| Muscular Dystrophy, Emery-Dreifuss \| Oculocerebrorenal Syndrome \| Pelizaeus-Merzbacher Disease \| X-Linked Combined Immunodeficiency Diseases \| Activated Protein C Resistance \| Antithrombin III Deficiency \| Hermanski-Pudlak Syndrome \| Protein C Deficiency \| Purpura, Thrombotic Thrombocytopenic \| Agammaglobulinemia \| Ataxia Telangiectasia \| Common Variable Immunodeficiency \| Deltaretrovirus Infections \| DiGeorge Syndrome \| Dysgammaglobulinemia \| HIV Infections \| Leukocyte-Adhesion Deficiency Syndrome \| Lymphopenia \| Phagocyte Bactericidal Dysfunction \| Severe Combined Immunodeficiency X
URI:	X
Termer och motsvarande begrepp:	Wiskott-Aldrichin oireyhtymä (fi) Wiskott-Aldrichin syndrooma (fi, ersatt) Wiskott-Aldrich Syndrome (en) Aldrich Syndrome (en, ersatt) Syndroma Wiskott-Aldrich (la-FI, ersatt) X
Dela:	X