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- Q6901244 subject Q5881496.
- Q6901244 subject Q6500135.
- Q6901244 subject Q7004986.
- Q6901244 subject Q7210495.
- Q6901244 subject Q8863634.
- Q6901244 abstract "The autosomal dominant syndrome associated with monocytopenia, B and NK cell lymphopenia and mycobacterial, fungal and viral infections (abbreviated MonoMAC) is a rare genetic disorder first described by Vihn and colleagues in 2010 and is associated with myelodysplasia, cytogenetic abnormalities, pulmonary alveolar proteinosis and myeloid leukemias. Multiple mutations in the GATA2 are considered to be responsible for this syndrome.".
- Q6901244 wikiPageWikiLink Q1072420.
- Q6901244 wikiPageWikiLink Q1137717.
- Q6901244 wikiPageWikiLink Q11688946.
- Q6901244 wikiPageWikiLink Q12078.
- Q6901244 wikiPageWikiLink Q1485.
- Q6901244 wikiPageWikiLink Q14914524.
- Q6901244 wikiPageWikiLink Q1504713.
- Q6901244 wikiPageWikiLink Q160105.
- Q6901244 wikiPageWikiLink Q18025461.
- Q6901244 wikiPageWikiLink Q180614.
- Q6901244 wikiPageWikiLink Q188930.
- Q6901244 wikiPageWikiLink Q200779.
- Q6901244 wikiPageWikiLink Q2303073.
- Q6901244 wikiPageWikiLink Q29496.
- Q6901244 wikiPageWikiLink Q3267926.
- Q6901244 wikiPageWikiLink Q332181.
- Q6901244 wikiPageWikiLink Q4301850.
- Q6901244 wikiPageWikiLink Q448698.
- Q6901244 wikiPageWikiLink Q485831.
- Q6901244 wikiPageWikiLink Q5881496.
- Q6901244 wikiPageWikiLink Q6500135.
- Q6901244 wikiPageWikiLink Q6531938.
- Q6901244 wikiPageWikiLink Q6900.
- Q6901244 wikiPageWikiLink Q7004986.
- Q6901244 wikiPageWikiLink Q7210495.
- Q6901244 wikiPageWikiLink Q8277.
- Q6901244 wikiPageWikiLink Q8863634.
- Q6901244 wikiPageWikiLink Q954625.
- Q6901244 wikiPageWikiLink Q979564.
- Q6901244 name "monoMAC syndrome".
- Q6901244 type Disease.
- Q6901244 type Thing.
- Q6901244 type Q12136.
- Q6901244 comment "The autosomal dominant syndrome associated with monocytopenia, B and NK cell lymphopenia and mycobacterial, fungal and viral infections (abbreviated MonoMAC) is a rare genetic disorder first described by Vihn and colleagues in 2010 and is associated with myelodysplasia, cytogenetic abnormalities, pulmonary alveolar proteinosis and myeloid leukemias. Multiple mutations in the GATA2 are considered to be responsible for this syndrome.".
- Q6901244 label "MonoMAC".
- Q6901244 name "monoMAC syndrome".