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- Hyper-IgM_syndrome_type_1 abstract "Hyper IgM Syndrome Type 1 is the X-linked variant of the Hyper-IgM syndrome. The affected individuals are virtually always male, because males only have one X chromosome, received from their mothers. Their mothers are not symptomatic, even though they are carriers of the allele, because the trait is recessive. Male offspring of these women have a 50% chance of inheriting their mother's mutant allele.".
- Hyper-IgM_syndrome_type_1 icd10 "D80.5".
- Hyper-IgM_syndrome_type_1 icd9 "279.05".
- Hyper-IgM_syndrome_type_1 meshId "D053307".
- Hyper-IgM_syndrome_type_1 wikiPageExternalLink dispomim.cgi?id=308230.
- Hyper-IgM_syndrome_type_1 wikiPageID "6886194".
- Hyper-IgM_syndrome_type_1 wikiPageLength "2669".
- Hyper-IgM_syndrome_type_1 wikiPageOutDegree "9".
- Hyper-IgM_syndrome_type_1 wikiPageRevisionID "642740863".
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink CD40.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink CD40_(protein).
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink Category:Immune_system_disorders.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink Gamma_globulin.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink Gammaglobulin.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink Hyper-IgM_syndrome.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink Hyper_IgM_syndrome.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink IgA.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink IgG.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink Immunoglobulin_A.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink Immunoglobulin_G.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink Ligand.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink Sex_linkage.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink X-linked.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLink X_chromosome.
- Hyper-IgM_syndrome_type_1 wikiPageWikiLinkText "1".
- Hyper-IgM_syndrome_type_1 wikiPageWikiLinkText "Hyper-IgM syndrome type 1".
- Hyper-IgM_syndrome_type_1 wikiPageWikiLinkText "Hyper-IgM_syndrome_type_1".
- Hyper-IgM_syndrome_type_1 hasPhotoCollection Hyper-IgM_syndrome_type_1.
- Hyper-IgM_syndrome_type_1 icd "279.05".
- Hyper-IgM_syndrome_type_1 icd "D80.5".
- Hyper-IgM_syndrome_type_1 meshid "D053307".
- Hyper-IgM_syndrome_type_1 name "Hyper-IgM syndrome type 1".
- Hyper-IgM_syndrome_type_1 wikiPageUsesTemplate Template:Immune_disorders.
- Hyper-IgM_syndrome_type_1 wikiPageUsesTemplate Template:Immunology-stub.
- Hyper-IgM_syndrome_type_1 wikiPageUsesTemplate Template:Infobox_disease.
- Hyper-IgM_syndrome_type_1 wikiPageUsesTemplate Template:Reflist.
- Hyper-IgM_syndrome_type_1 wikiPageUsesTemplate Template:X-linked_disorders.
- Hyper-IgM_syndrome_type_1 subject Category:Immune_system_disorders.
- Hyper-IgM_syndrome_type_1 hypernym 039;.
- Hyper-IgM_syndrome_type_1 type Disease.
- Hyper-IgM_syndrome_type_1 type Disorder.
- Hyper-IgM_syndrome_type_1 type Thing.
- Hyper-IgM_syndrome_type_1 type Q12136.
- Hyper-IgM_syndrome_type_1 comment "Hyper IgM Syndrome Type 1 is the X-linked variant of the Hyper-IgM syndrome. The affected individuals are virtually always male, because males only have one X chromosome, received from their mothers. Their mothers are not symptomatic, even though they are carriers of the allele, because the trait is recessive. Male offspring of these women have a 50% chance of inheriting their mother's mutant allele.".
- Hyper-IgM_syndrome_type_1 label "Hyper-IgM syndrome type 1".
- Hyper-IgM_syndrome_type_1 sameAs m.0gv999.
- Hyper-IgM_syndrome_type_1 sameAs Q8041555.
- Hyper-IgM_syndrome_type_1 sameAs Q8041555.
- Hyper-IgM_syndrome_type_1 wasDerivedFrom Hyper-IgM_syndrome_type_1?oldid=642740863.
- Hyper-IgM_syndrome_type_1 isPrimaryTopicOf Hyper-IgM_syndrome_type_1.
- Hyper-IgM_syndrome_type_1 name "Hyper-IgM syndrome type 1".