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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: Fibrosis (D005355)
Parent Node: Peritoneal Diseases (D010532)
..Starting node ..Peritoneal Fibrosis (D056627)
Child Nodes:
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:	8825
Name:	Peritoneal Fibrosis
Definition:	Disorder characterized by a wide range of structural changes in PERITONEUM, resulting from fibrogenic or inflammatory processes. Peritoneal fibrosis is a common complication in patients receiving PERITONEAL DIALYSIS and contributes to its gradual decrease in efficiency.
Alternative IDs:
ParentIDs:	MESH:D005355\|MESH:D010532
TreeNumbers:	C06.844.610 \|C23.550.355.625
Synonyms:	Encapsulating Peritoneal Scleroses \|Encapsulating Peritoneal Sclerosis \|Fibroses, Peritoneal \|Fibrosing Syndrome, Peritoneal \|Fibrosing Syndromes, Peritoneal \|Fibrosis, Peritoneal \|Peritoneal Fibroses \|Peritoneal Fibrosing Syndrome \|Peritoneal Fibrosing Syndrome
Slim Mappings:	Digestive system disease\|Pathology (process)
Reference:	MedGen: D056627 MeSH: D056627 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants