MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation 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

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: adenoma (MONDO:0004972)
Parent Node: benign epithelial neoplasm (MONDO:0036976)
Parent Node: glandular cell neoplasm (MONDO:0024276)
Parent Node: ovarian benign neoplasm (MONDO:0000646)
Parent Node: ovarian epithelial tumor (MONDO:0002229)
Parent Node: rete ovarii neoplasm (MONDO:0003192)
..Starting node ..rete ovarii adenoma ()
Child Nodes:
........rete ovarii cystadenoma ()
Sister Nodes:
..rete ovarii adenocarcinoma ()
..rete ovarii adenoma ()
..rete ovarii cystadenofibroma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4005
Name:	rete ovarii adenoma
Definition:	An adenoma that arises from the rete ovarii. It is composed of elongated tubules. The clinical course is benign.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenoma, rete ovarii, benign; rete ovarii adenoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal