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: breast neoplasm (MONDO:0021100)
Parent Node: thoracic benign neoplasm (MONDO:0000634)
..Starting node ..breast benign neoplasm ()
Child Nodes:
........Becker nevus syndrome ()
........benign breast adenomyoepithelioma ()
........benign breast phyllodes tumor ()
........benign eccrine breast spiradenoma ()
........benign neoplasm of male breast ()
........breast adenoma ()
........breast cyst ()
........breast fibroadenoma ()
........breast fibroadenosis ()
........breast hemangioma ()
........breast leiomyoma ()
........breast lipoma ()
........breast myofibroblastoma ()
........breast papillomatosis ()
........diabetic mastopathy ()
........giant adenofibroma of the breast ()
........intraductal breast papilloma ()
........multiple fibroadenoma of the breast ()
Sister Nodes:
..benign axillary neoplasm ()
..benign neoplasm of chest wall ()
..benign neoplasm of esophagus ()
..benign neoplasm of heart ()
..benign neoplasm of mediastinum ()
..benign neoplasm of pericardium ()
..benign neoplasm of sternum ()
..benign neoplasm of thymus ()
..breast benign neoplasm ()
..endobronchial lipoma ()
..lung benign neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	620
Name:	breast benign neoplasm
Definition:	A non-metastasizing neoplasm arising from the breast parenchyma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign breast neoplasm; benign breast tumor; benign neoplasm of breast; benign neoplasm of the breast; benign tumor of breast; benign tumor of the breast; breast benign neoplasm
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal