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: carcinoma of urethra (MONDO:0021327)
..Starting node ..urethra adenocarcinoma ()
Child Nodes:
........urethra clear cell adenocarcinoma ()
Sister Nodes:
..carcinoma in situ of urethra ()
..Littre gland carcinoma ()
..urethra adenocarcinoma ()
..urethra squamous cell carcinoma ()
..urethra transitional cell carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3200
Name:	urethra adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the urethra
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of the urethra; adenocarcinoma of urethra; UAD; urethra adenocarcinoma; urethral adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: DSPP;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal