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: adenocarcinoma (MONDO:0004970)
Parent Node: skin appendage carcinoma (MONDO:0006973)
Parent Node: sweat gland cancer (MONDO:0002206)
..Starting node ..sweat gland carcinoma ()
Child Nodes:
........apocrine adenocarcinoma ()
........cutaneous adenocystic carcinoma ()
........eccrine carcinoma ()
........hidradenocarcinoma ()
Sister Nodes:
..apocrine sweat gland cancer ()
..eccrine sweat gland cancer ()
..malignant syringoma ()
..sweat gland carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5524
Name:	sweat gland carcinoma
Definition:	A carcinoma arising from the sweat glands. Representative examples include tubular carcinoma, spiradenocarcinoma, eccrine carcinoma, hidradenocarcinoma, and apocrine carcinoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	carcinoma of sweat gland; carcinoma of the sweat gland; carcinoma, sweat gland, malignant; sweat gland carcinoma; sweat gland carcinoma/apocrine eccrine carcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal