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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Adenomatous Polyposis Coli (D011125)
..Starting node ..Attenuated familial adenomatous polyposis (C538265)
Child Nodes:
Sister Nodes:
..Attenuated familial adenomatous polyposis (C538265)
..Colorectal Adenomatous Polyposis, Autosomal Recessive (C563924)
..Desmoid disease, hereditary (C535944)
..Gardner Syndrome (D005736) 3
..Leukemia, Acute Myelocytic, with Polyposis Coli and Colon Cancer (C565441)
..Polyposis Syndrome, Hereditary Mixed, 1 (C563365)
..Polyposis Syndrome, Hereditary Mixed, 2 (C566451)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1053
Name:	Attenuated familial adenomatous polyposis
Definition:
Alternative IDs:
ParentIDs:	MESH:D011125
TreeNumbers:	C04.557.470.035.215.100/C538265 \|C04.588.274.476.411.307.089/C538265 \|C04.588.274.476.411.307.180.089/C538265 \|C04.700.100/C538265 \|C06.301.371.411.307.180.089/C538265 \|C06.405.249.411.307.180.089/C538265 \|C06.405.469.158.356.180.089/C538265 \|C06.405.469.491.30
Synonyms:	Familial Adenomatous Polyposis, Attenuated
Slim Mappings:	Cancer\|Digestive system disease\|Genetic disease (inborn)
Reference:	MedGen: C538265 MeSH: C538265 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants