Disease browser and phenotype portal

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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: Abdominal Neoplasms (D000008)
Parent Node: Digestive System Neoplasms (D004067)
Parent Node: Peritoneal Diseases (D010532)
..Starting node ..Peritoneal Neoplasms (D010534)
Child Nodes:
........Mesenteric Cyst (D008639)
Sister Nodes:
..Chylous Ascites (D002915) 1
..Hemoperitoneum (D006465)
..Mesenteric Ischemia (D065666)
..Mesenteric Lymphadenitis (D008640)
..Mesenteric Vascular Occlusion (D008641)
..Panniculitis, Peritoneal (D015436) 1
..Peritoneal Fibrosis (D056627)
..Peritoneal Neoplasms (D010534) 1
..Peritonitis (D010538) 3
..Pneumoperitoneum (D011027)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8826
Name:	Peritoneal Neoplasms
Definition:	Tumors or cancer of the PERITONEUM.
Alternative IDs:
ParentIDs:	MESH:D000008\|MESH:D004067\|MESH:D010532
TreeNumbers:	C04.588.033.513 \|C04.588.274.780 \|C06.301.780 \|C06.844.620
Synonyms:	Neoplasm, Peritoneal \|Neoplasms, Peritoneal \|Peritoneal Neoplasm
Slim Mappings:	Cancer\|Digestive system disease
Reference:	MedGen: D010534 MeSH: D010534 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants