Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Splenic Diseases (D013158)
..Starting node ..Wandering Spleen (D050805)
Child Nodes:
Sister Nodes:
..Heterotaxy Syndrome (D059446) 7
..Hypersplenism (D006971) 1
..Splenic Infarction (D013159)
..Splenic Neoplasms (D013160) 1
..Splenic Rupture (D013161) 1
..Tuberculosis, Splenic (D014400)
..Wandering Spleen (D050805)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11699
Name:	Wandering Spleen
Definition:	A congenital or acquired condition in which the SPLEEN is not in its normal anatomical position but moves about in the ABDOMEN. This is due to laxity or absence of suspensory ligaments which normally provide peritoneal attachments to keep the SPLEEN in a fixed position. Clinical symptoms include ABDOMINAL PAIN, splenic torsion and ISCHEMIA.
Alternative IDs:
ParentIDs:	MESH:D013158
TreeNumbers:	C15.604.744.954
Synonyms:	Displaced Spleen \|Displaced Spleens \|Drifting Spleen \|Drifting Spleens \|Floating Spleen \|Floating Spleens \|Ptoses, Splenic \|Ptosis, Splenic \|Spleen, Displaced \|Spleen, Drifting \|Spleen, Floating \|Spleens, Displaced \|Spleens, Drifting \|Spleens, Floating \|Spleens, Wande
Slim Mappings:	Lymphatic disease
Reference:	MedGen: D050805 MeSH: D050805 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants