Disease browser and phenotype 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

Disease Browser
Parent Node: Breast Diseases (D001941)
..Starting node ..Polythelia, Familial (C562557)
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:	9119
Name:	Polythelia, Familial
Definition:
Alternative IDs:
ParentIDs:	MESH:D001941
TreeNumbers:	C17.800.090/C562557
Synonyms:	Accessory Nipples \|Nipples, Supernumerary \|Polymastia
Slim Mappings:	Skin disease
Reference:	MedGen: C562557 MeSH: C562557 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants