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: glandular cell neoplasm (MONDO:0024276)
..Starting node ..serous neoplasm ()
Child Nodes:
........ovarian serous tumor ()
Sister Nodes:
..adenocarcinoma ()
..cystadenoma ()
..glandular papilloma ()
..mucinous neoplasm ()
..oncocytic neoplasm () L: 00167;
..rete ovarii adenoma ()
..serous neoplasm ()
..vaginal glandular neoplasm ()
..villous adenoma ()
..vulvar glandular neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	37256
Name:	serous neoplasm
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	serous neoplasm
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal