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: neoplasm of testis (MONDO:0021348)
..Starting node ..rete testis neoplasm ()
Child Nodes:
........rete testis adenocarcinoma ()
........rete testis adenoma ()
Sister Nodes:
..benign neoplasm of testis ()
..childhood testicular neoplasm ()
..rete testis neoplasm ()
..seminal vesicle tumor ()
..testicular Brenner tumor ()
..testicular cancer ()
..testicular germ cell tumor ()
..testicular sex cord-stromal neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3562
Name:	rete testis neoplasm
Definition:	A benign or malignant neoplasm that affects the rete testis. Representative examples include adenoma and adenocarcinoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	neoplasm of rete testis; rete testis neoplasm; rete testis neoplasm (disease); rete testis tumor; tumor of rete testis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: TAF1;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal