adenomatous polyposis coli

Preferred Label : adenomatous polyposis coli;

MeSH definition : A polyposis syndrome due to an autosomal dominant mutation of the APC genes (GENES, APC) on CHROMOSOME 5. The syndrome is characterized by the development of hundreds of ADENOMATOUS POLYPS in the COLON and RECTUM of affected individuals by early adulthood.;

MeSH synonym : familial adenomatous polyposis coli; familial polyposis coli; familial polyposis syndrome; adenomatous polyposis, familial; polyposis coli, familial; adenomatous polyposis coli, familial; adenomatous polyposis of the colon; Hereditary Polyposis Colus; Polyposis Coli, Hereditary; Polyposis Colus, Hereditary; Familial Adenomatous Polyposis of the Colon; Colus, Hereditary Polyposis; Adenomatous Polyposis Colus; Coli, Adenomatous Polyposis; Colus, Adenomatous Polyposis; Polyposis Coli, Adenomatous; Polyposis Colus, Adenomatous; familial adenomatous polyposis; Adenomatous Polyposes, Familial; Familial Adenomatous Polyposes; Polyposes, Familial Adenomatous; Polyposis, Familial Adenomatous; polyposis syndrome, familial; Familial Polyposis Syndromes; Familial Multiple Polyposi; Familial Multiple Polyposus; Multiple Polyposi, Familial; Multiple Polyposus, Familial; Polyposi, Familial Multiple; Polyposus, Familial Multiple; Coli, Familial Polyposis; Colus, Familial Polyposis; Familial Polyposis Colus; Polyposis Colus, Familial; Familial Polyposis of the Colon; Hereditary Polyposis Coli; Coli, Hereditary Polyposis; familial multiple polyposis; familial multiple polyposes; multiple polyposes, familial; multiple polyposis, familial; polyposes, familial multiple; polyposis, familial multiple; familial multiple polyposis syndrome; Myh-Associated polyposis; myh associated polyposis; Myh-Associated polyposes; polyposes, Myh-Associated; polyposis, Myh-Associated; polyposis coli; coli, polyposis; colus, polyposis; polyposis colus;

CISMeF acronym : APC;

Related MeSH term : polyposis, adenomatous intestinal; familial intestinal polyposis; Familial Intestinal Polyposes; Intestinal Polyposes, Familial; Intestinal Polyposis, Familial; Adenomatous Intestinal Polyposes; Adenomatous Intestinal Polyposis; Intestinal Polyposis, Adenomatous;

Wikipedia link : https://en.wikipedia.org/wiki/Apc;

Details

Origin ID

D011125;

UMLS CUI

C0032580;

Allowable qualifiers
- blood [MeSH Qualifier]
- blood supply [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- chemistry [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- secondary [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- ultrastructure [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- APC [ICHI extension code]
- APC Gene [NCIt concept]
- APC regulator of WNT signaling pathway [ORDO Gene]
- Absolute Phagocyte Count [NCIt concept]
- Adenomatous Polyposis Coli Protein [NCIt concept]
- Alkylphosphocholine Compound [NCIt concept]
- Antigen Presenting Cell [NCIt concept]
- Apc regulator of wnt signaling pathway [OMIM gene]
- Argon Beam Coagulator Ablation [NCIt concept]
- Atrial Premature Complex by ECG Finding [NCIt concept]
- PROC wt Allele [NCIt concept]
- Paroxysmal atrial fibrillation (disorder) [SNOMED CT concept]
- anaphase-promoting complex [GO term]
Currated CISMeF NLP mapping
- Adenomatous polyposis coli [ICD-O code]
- Adenomatous polyposis coli [ICD-11 Extension code]
- Adenomatous polyposis coli [MedDRA Preferred Term]
- Adenomatous polyposis coli [ICD-9 code]
- Adenomatous polyposis coli (morphologic abnormality) [SNOMED CT concept]
- Familial Adenomatous Polyposis [NCIt concept]
- Familial adenomatous polyposis [Vue CIM-11]
- Familial adenomatous polyposis [TUV Concept]
- Familial adenomatous polyposis [OMIM phenotypic series]
- Familial adenomatous polyposis [ORDO Disease]
- Familial adenomatous polyposis [MedDRA LLT]
- Familial adenomatous polyposis 1 [OMIM Phenotype]
- Familial adenomatous polyposis coli [PASCAL descriptor]
- Familial multiple polyposis syndrome (disorder) [SNOMED CT concept]
- Familial polyposis [MedDRA LLT]
- MYH-associated polyposis (disorder) [SNOMED CT concept]
- Polyposis coli [MedDRA LLT]
- adenomatous polyposis coli [Disease (Nov.)]
- adenomatous polyposis coli [SNOMED Notion]
- familial adenomatous polyposis [DO Concept]
- familial multiple polyposis syndrome [SNOMED Notion]
DO Cross reference
- familial adenomatous polyposis [DO Concept]
False automatic mappings
- APC [ICD-11 Extension code]
Manual BTNT mappings - CISMeF
- Turcot syndrome with polyposis [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Inherited cancer-predisposing syndrome [ORDO Disease]
ORDO relation(s)
- Familial adenomatous polyposis [ORDO Disease]
Record concept(s)
- adenomatous polyposis coli [MeSH concept]
- familial intestinal polyposis [MeSH concept]
- polyposis, adenomatous intestinal [MeSH concept]
Related MeSH Supplementary Concept(s)
- attenuated familial adenomatous polyposis [MeSH Supplementary Concept]
- colorectal adenomatous polyposis, autosomal recessive [MeSH Supplementary Concept]
- desmoid disease, hereditary [MeSH Supplementary Concept]
- leukemia, acute myelocytic, with polyposis coli and colon cancer [MeSH Supplementary Concept]
- polyposis syndrome, hereditary mixed, 1 [MeSH Supplementary Concept]
- polyposis syndrome, hereditary mixed, 2 [MeSH Supplementary Concept]
See also
- adenomatous polyposis coli protein [MeSH Descriptor]
- gardner syndrome [MeSH Descriptor]
- genes, apc [MeSH Descriptor]
See also (suggested by CISMeF)
- intestinal polyps [MeSH Descriptor]
See also inter- (CISMeF)
- MUTYH-Associated Polyposis [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Adenomatous polyposis coli [MedDRA Preferred Term]
- Adenomatous polyposis coli [ICD-9 code]
- Adenomatous polyposis coli [ICD-O code]
- Adenomatous polyposis coli (morphologic abnormality) [SNOMED CT concept]
- Familial Adenomatous Polyposis [NCIt concept]
- Familial adenomatous polyposis [MedDRA LLT]
- Familial adenomatous polyposis [ORDO Disease]
- Familial adenomatous polyposis [TUV Concept]
- Familial adenomatous polyposis 1 [OMIM Phenotype]
- Familial multiple polyposis syndrome (disorder) [SNOMED CT concept]
- Familial polyposis [MedDRA LLT]
- MYH-associated polyposis (disorder) [SNOMED CT concept]
- Polyposis coli [MedDRA LLT]
- adenomatous polyposis coli [Disease (Nov.)]
- adenomatous polyposis coli [SNOMED Notion]
- familial adenomatous polyposis [DO Concept]
- familial multiple polyposis syndrome [SNOMED Notion]
Validated automatic mappings to NTBT
- Adenomatous colonic polyposis [HPO term]
- Adenomatous polyp of the colon [ICD-11 More detail]
- Genetic intestinal polyposis [ORDO Disease]

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