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: adenocarcinoma (MONDO:0004970)
Parent Node: urinary bladder carcinoma (MONDO:0004986)
..Starting node ..bladder adenocarcinoma ()
Child Nodes:
........bladder clear cell adenocarcinoma ()
........bladder colloid adenocarcinoma ()
........bladder colonic type adenocarcinoma ()
........bladder hepatoid adenocarcinoma ()
........bladder mixed adenocarcinoma ()
........bladder signet ring cell adenocarcinoma ()
........bladder urachal adenocarcinoma ()
Sister Nodes:
..bladder adenocarcinoma ()
..bladder squamous cell carcinoma ()
..bladder transitional cell carcinoma ()
..bladder urachal carcinoma ()
..childhood bladder carcinoma ()
..stage IVb bladder cancer ()
..superficial urinary bladder carcinoma ()
..urinary bladder small cell neuroendocrine carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2751
Name:	bladder adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the urinary bladder
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of bladder; adenocarcinoma of the bladder; adenocarcinoma of the urinary bladder; adenocarcinoma of urinary bladder; blad; bladder adenocarcinoma; bladder adenocarcinoma, not otherwise specified; urinary bladder adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: KERA;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal