MUTYH-associated polyposis

MUTYH-associated polyposis: MYH-associated polyposis an autosomal recessive disorder closely resembling familial adenomatous polyposis but caused by homozygous mutations in the MUTYH gene (locus: 1p34.3-p32.1), which is involved in mismatch repair.

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MUTYH-assoziierte Polyposis — Klassifikation nach ICD 10 D12 Gutartige Neubildung des Kolons, des Rektums, des Analkanals und des Anus D12.6 Kolon, nicht näher bezeichnet Polyposis coli (hereditär) … Deutsch Wikipedia
MUTYH — (mutY Homolog (E. coli)) is a human gene cite web | title = Entrez Gene: MUTYH mutY homolog (E. coli)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=4595| accessdate = ] that carries the instructions for… … Wikipedia
autosomal recessive colorectal adenomatous polyposis — MUTYH associated p … Medical dictionary
Familial adenomatous polyposis — Classification and external resources Endoscopic image of sigmoid colon of patient with familial adenomatous polyposis. ICD 10 C … Wikipedia
Sine qua non — For other uses, see Sine qua non (disambiguation). Sine qua non (pronounced /ˌsaɪnɨ kweɪ ˈnɒn/, Latin: [ˈsine kwaː ˈnoːn])[1] or condicio sine qua non (plural: condiciones sine quibus non) refers to an indispensable and essential action,… … Wikipedia
AXIN2 — Axin 2 (conductin, axil), also known as AXIN2, is a human gene.cite web | title = Entrez Gene: AXIN2 axin 2 (conductin, axil)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=8313| accessdate = ] PBB Summary … Wikipedia

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