obsolete_MUTYH-related attenuated familial adenomatous polyposis https://rarediseases.info.nih.gov/diseases/10805/myh-associated-polyposis true MAP syndrome FAP2 UMLS:C1837991 familial adenomatous polyposis 2 http://purl.obolibrary.org/obo/MONDO_0012041 MUTYH-related AFAP MUTYH-related attenuated familial adenomatous polyposis Replaced with Mondo term. MAP autosomal recessive multiple colorectal adenomas MUTYH-associated polyposis NCIT:C96520 GARD:0010805 MYH-associated polyposis MUTYH-related attenuated familial polyposis coli autosomal recessive familial adenomatous polyposis familial adenomatous polyposis, 2 Orphanet:247798 OMIM:608456 familial adenomatous polyposis, type 2 MESH:C563924 colorectal adenomatous polyposis, autosomal recessive adenomas, multiple colorectal, autosomal recessive An autosomal recessive hereditary neoplastic syndrome caused by mutations in the MUTYH gene on chromosome 1p34.1. It is characterized by the presence of multiple colorectal polyps that may progress to carcinoma. Development of gastric and small intestinal polyps may also occur. MUTYH-related attenuated FAP 3.41.0 ICD10:D12.6