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: penile carcinoma (MONDO:0006360)
..Starting node ..adenocarcinoma of penis ()
Child Nodes:
........Paget disease of the penis ()
Sister Nodes:
..adenocarcinoma of penis ()
..penis basal cell carcinoma ()
..squamous cell carcinoma of penis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	18351
Name:	adenocarcinoma of penis
Definition:	A adenocarcinoma that involves the penis.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of the penis; penile adenocarcinoma; penis adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal