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: benign neoplasm of skin (MONDO:0021440)
Parent Node: sweat gland neoplasm (MONDO:0002381)
..Starting node ..benign neoplasm of sweat gland ()
Child Nodes:
........adnexal spiradenoma/cylindroma of a sweat gland ()
........benign eccrine neoplasm ()
........benign spiradenoma ()
........breast apocrine adenoma ()
........eccrine acrospiroma ()
........hidrocystoma ()
........vulvar nodular hidradenoma ()
........vulvar syringoma ()
Sister Nodes:
..apocrine sweat gland neoplasm ()
..benign neoplasm of sweat gland ()
..eccrine sweat gland neoplasm ()
..sweat gland adenoma ()
..sweat gland cancer ()
..syringoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21489
Name:	benign neoplasm of sweat gland
Definition:	A benign neoplasm that involves the sweat gland.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign neoplasm of the sweat gland; benign sweat gland neoplasm; benign sweat gland tumor; benign tumor of sweat gland; benign tumor of the sweat gland; sweat gland benign neoplasm; sweat gland neoplasm, benign
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal