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: connective tissue cancer (MONDO:0002176)
..Starting node ..scirrhous adenocarcinoma ()
Child Nodes:
Sister Nodes:
..bone cancer ()
..cholangiolocellular carcinoma ()
..chondrosarcoma (disease) ()
..fibrosarcoma (disease) ()
..lipomatous cancer ()
..malignant peritoneal solitary fibrous tumor ()
..malignant pleural solitary fibrous tumor ()
..scirrhous adenocarcinoma ()
..synovium cancer ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5953
Name:	scirrhous adenocarcinoma
Definition:	An infiltrating adenocarcinoma characterized by the presence of desmoplastic stromal reaction.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma with productive fibrosis; FIBROADENOCARCINOMA, malignant; fibrocarcinoma; scirrhous adenocarcinoma; scirrhous adenocarcinoma (morphologic abnormality); scirrhous carcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal