Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Omenn_syndrome> ?p ?o }
Showing triples 1 to 86 of
86
with 100 triples per page.
- Omenn_syndrome abstract "Omenn syndrome is an autosomal recessive severe combined immunodeficiency associated with hypomorphic missense mutations in immunologically relevant genes of T-cells (and B-cells) as recombination activating genes (RAG1 and RAG2), IL-7 Receptor α gene (IL7Rα), DCLRE1C-Artemis, RMRP-CHH, DNA-Ligase IV, common gamma chain, WHN-FOXN1, ZAP-70 and complete DiGeorge anomaly (DiGeorge Syndrome; CHARGE).".
- Omenn_syndrome icd10 "D81.2(ILDSD81.210)".
- Omenn_syndrome omim "603554".
- Omenn_syndrome thumbnail Omenn_syndrome.png?width=300.
- Omenn_syndrome wikiPageID "2294715".
- Omenn_syndrome wikiPageLength "4685".
- Omenn_syndrome wikiPageOutDegree "43".
- Omenn_syndrome wikiPageRevisionID "694026348".
- Omenn_syndrome wikiPageWikiLink Antibody.
- Omenn_syndrome wikiPageWikiLink B-cell_receptor.
- Omenn_syndrome wikiPageWikiLink B_cell.
- Omenn_syndrome wikiPageWikiLink Category:Autosomal_recessive_disorders.
- Omenn_syndrome wikiPageWikiLink Category:Combined_T_and_B–cell_immunodeficiencies.
- Omenn_syndrome wikiPageWikiLink Category:Hepatology.
- Omenn_syndrome wikiPageWikiLink Category:Noninfectious_immunodeficiency-related_cutaneous_conditions.
- Omenn_syndrome wikiPageWikiLink Category:Rare_diseases.
- Omenn_syndrome wikiPageWikiLink Category:Syndromes.
- Omenn_syndrome wikiPageWikiLink Common_gamma_chain.
- Omenn_syndrome wikiPageWikiLink DCLRE1C.
- Omenn_syndrome wikiPageWikiLink DNA_repair_protein_XRCC4.
- Omenn_syndrome wikiPageWikiLink DiGeorge_syndrome.
- Omenn_syndrome wikiPageWikiLink Diarrhea.
- Omenn_syndrome wikiPageWikiLink Dominance_(genetics).
- Omenn_syndrome wikiPageWikiLink Eosinophilia.
- Omenn_syndrome wikiPageWikiLink Erythroderma.
- Omenn_syndrome wikiPageWikiLink FOXN1.
- Omenn_syndrome wikiPageWikiLink Failure_to_thrive.
- Omenn_syndrome wikiPageWikiLink File:Autorecessive.svg.
- Omenn_syndrome wikiPageWikiLink Graft-versus-host_disease.
- Omenn_syndrome wikiPageWikiLink Hematopoietic_stem_cell_transplantation.
- Omenn_syndrome wikiPageWikiLink Hepatomegaly.
- Omenn_syndrome wikiPageWikiLink Immunoglobulin_E.
- Omenn_syndrome wikiPageWikiLink Interleukin-7_receptor-α.
- Omenn_syndrome wikiPageWikiLink List_of_cutaneous_conditions.
- Omenn_syndrome wikiPageWikiLink Lymphadenopathy.
- Omenn_syndrome wikiPageWikiLink Missense_mutation.
- Omenn_syndrome wikiPageWikiLink Mullers_morphs.
- Omenn_syndrome wikiPageWikiLink Opportunistic_infection.
- Omenn_syndrome wikiPageWikiLink Purine_nucleoside_phosphorylase_deficiency.
- Omenn_syndrome wikiPageWikiLink RMRP.
- Omenn_syndrome wikiPageWikiLink Recombination-activating_gene.
- Omenn_syndrome wikiPageWikiLink Severe_combined_immunodeficiency.
- Omenn_syndrome wikiPageWikiLink Splenomegaly.
- Omenn_syndrome wikiPageWikiLink T_cell.
- Omenn_syndrome wikiPageWikiLink T_cell_receptor.
- Omenn_syndrome wikiPageWikiLink The_International_League_of_Dermatological_Societies.
- Omenn_syndrome wikiPageWikiLink ZAP70.
- Omenn_syndrome wikiPageWikiLink File:Omenn_syndrome.png.
- Omenn_syndrome wikiPageWikiLinkText "Omenn syndrome".
- Omenn_syndrome diseasesdb "32676".
- Omenn_syndrome emedicinesubj "ped".
- Omenn_syndrome emedicinetopic "1640".
- Omenn_syndrome icd "D81.2".
- Omenn_syndrome mesh "D016511".
- Omenn_syndrome name "Omenn syndrome".
- Omenn_syndrome omim "603554".
- Omenn_syndrome orphanet "39041".
- Omenn_syndrome wikiPageUsesTemplate Template:Immune_disorders.
- Omenn_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Omenn_syndrome wikiPageUsesTemplate Template:Reflist.
- Omenn_syndrome subject Category:Autosomal_recessive_disorders.
- Omenn_syndrome subject Category:Combined_T_and_B–cell_immunodeficiencies.
- Omenn_syndrome subject Category:Hepatology.
- Omenn_syndrome subject Category:Noninfectious_immunodeficiency-related_cutaneous_conditions.
- Omenn_syndrome subject Category:Rare_diseases.
- Omenn_syndrome subject Category:Syndromes.
- Omenn_syndrome hypernym Immunodeficiency.
- Omenn_syndrome type Disease.
- Omenn_syndrome type Disorder.
- Omenn_syndrome type Specialty.
- Omenn_syndrome type Syndrome.
- Omenn_syndrome type Thing.
- Omenn_syndrome type Q12136.
- Omenn_syndrome comment "Omenn syndrome is an autosomal recessive severe combined immunodeficiency associated with hypomorphic missense mutations in immunologically relevant genes of T-cells (and B-cells) as recombination activating genes (RAG1 and RAG2), IL-7 Receptor α gene (IL7Rα), DCLRE1C-Artemis, RMRP-CHH, DNA-Ligase IV, common gamma chain, WHN-FOXN1, ZAP-70 and complete DiGeorge anomaly (DiGeorge Syndrome; CHARGE).".
- Omenn_syndrome label "Omenn syndrome".
- Omenn_syndrome sameAs Q2214419.
- Omenn_syndrome sameAs Síndrome_de_Omenn.
- Omenn_syndrome sameAs Syndroom_van_Omenn.
- Omenn_syndrome sameAs Zespół_Omenna.
- Omenn_syndrome sameAs m.071l_y.
- Omenn_syndrome sameAs Sindromul_Omenn.
- Omenn_syndrome sameAs Q2214419.
- Omenn_syndrome wasDerivedFrom Omenn_syndrome?oldid=694026348.
- Omenn_syndrome depiction Omenn_syndrome.png.
- Omenn_syndrome isPrimaryTopicOf Omenn_syndrome.
- Omenn_syndrome name "Omenn syndrome".