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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

Disease Browser
Parent Node: Breast Diseases (D001941)
..Starting node ..Fibrocystic Breast Disease (D005348)
Child Nodes:
Sister Nodes:
..Amastia (C562989)
..Breast Cyst (D047688) 1
..Breast Neoplasms (D001943) 17
..Fibrocystic Breast Disease (D005348)
..Gynecomastia (D006177) 7
..Lactation Disorders (D007775) 5
..MAMMARY-DIGITAL-NAIL SYNDROME (OMIM:613689)
..Mastitis (D008413) 1
..Polythelia, Familial (C562557)
..Pseudoangiomatous stromal hyperplasia (C535824)
..Sclerosing lymphocytic lobulitis (C537524)
..Symmastia (C538147)
..Ulnar-mammary syndrome (C536937)
..Zuska's Disease (C536730)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4271
Name:	Fibrocystic Breast Disease
Definition:	A common and benign breast disease characterized by varying degree of fibrocystic changes in the breast tissue. There are three major patterns of morphological changes, including FIBROSIS, formation of CYSTS, and proliferation of glandular tissue (adenosis). The fibrocystic breast has a dense irregular, lumpy, bumpy consistency.
Alternative IDs:
ParentIDs:	MESH:D001941
TreeNumbers:	C17.800.090.750
Synonyms:	Adenoses, Microglandular \|Adenosis, Microglandular \|Adenosis of Breast \|Breast Adenosis \|Breast Cystic Disease \|Breast Cystic Diseases \|Breast Disease, Cystic \|Breast Disease, Fibrocystic \|Breast Dysplasia \|Breast Fibrocystic Change \|Breast Fibrocystic Changes \|Bre
Slim Mappings:	Skin disease
Reference:	MedGen: D005348 MeSH: D005348 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants