MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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: degenerative disorder (MONDO:0024236)
Parent Node: prostate disease (MONDO:0003105)
..Starting node ..atrophy of prostate ()
Child Nodes:
Sister Nodes:
..atrophy of prostate ()
..benign prostatic hyperplasia (disease) ()
..prostate calculus ()
..prostate neoplasm ()
..prostatic cyst ()
..prostatitis (disease) ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2264
Name:	atrophy of prostate
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	atrophic prostate; atrophy of prostate; prostate atrophy
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal