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- Q3508611 subject Q7004986.
- Q3508611 abstract "Hyper IgM Syndrome Type 1 (HIGM-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.".
- Q3508611 icd10 "D80.5".
- Q3508611 icd9 "279.05".
- Q3508611 meshId "D053307".
- Q3508611 wikiPageExternalLink dispomim.cgi?id=308230.
- Q3508611 wikiPageWikiLink Q1142188.
- Q3508611 wikiPageWikiLink Q1617658.
- Q3508611 wikiPageWikiLink Q17859635.
- Q3508611 wikiPageWikiLink Q193161.
- Q3508611 wikiPageWikiLink Q5520338.
- Q3508611 wikiPageWikiLink Q61333.
- Q3508611 wikiPageWikiLink Q7004986.
- Q3508611 wikiPageWikiLink Q79448.
- Q3508611 wikiPageWikiLink Q79453.
- Q3508611 icd "279.05".
- Q3508611 icd "D80.5".
- Q3508611 meshid "D053307".
- Q3508611 name "Hyper-IgM syndrome type 1".
- Q3508611 type Disease.
- Q3508611 type Thing.
- Q3508611 type Q12136.
- Q3508611 comment "Hyper IgM Syndrome Type 1 (HIGM-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.".
- Q3508611 label "Hyper-IgM syndrome type 1".
- Q3508611 name "Hyper-IgM syndrome type 1".