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: breast carcinoma (MONDO:0004989)
Parent Node: integumentary system cancer (MONDO:0000653)
..Starting node ..breast adenocarcinoma ()
Child Nodes:
........adenoid cystic breast carcinoma ()
........breast ductal adenocarcinoma ()
........breast lobular carcinoma ()
........breast malignant eccrine spiradenoma ()
........breast mucinous cystadenocarcinoma ()
........inflammatory breast carcinoma ()
........lobular breast carcinoma in situ ()
........mammary Paget disease ()
........mixed lobular and ductal breast carcinoma ()
........mucoepidermoid breast carcinoma ()
........oncocytic breast carcinoma ()
........sebaceous breast carcinoma ()
........signet ring cell breast carcinoma ()
Sister Nodes:
..atypical lobular breast hyperplasia ()
..bartholin gland carcinoma ()
..breast adenocarcinoma ()
..breast diffuse large B-cell lymphoma ()
..breast mucosa-associated lymphoid tissue lymphoma ()
..cornea cancer ()
..lip cancer ()
..skin cancer ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4988
Name:	breast adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the breast
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of breast; adenocarcinoma of the breast; breast adenocarcinoma; mammary adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal