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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)
Parent Node: Puerperal Disorders (D011644)
..Starting node ..Lactation Disorders (D007775)
Child Nodes:
........Galactorrhea (D005687) 3
........Prolactin Deficiency, Isolated (C562708)
Sister Nodes:
..Depression, Postpartum (D019052)
..Lactation Disorders (D007775) 5
..Mastitis (D008413) 1
..Postpartum Hemorrhage (D006473)
..Postpartum Thyroiditis (D050032)
..Pubic Symphysis Diastasis (D046548)
..Puerperal Infection (D011645)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6173
Name:	Lactation Disorders
Definition:	Disturbances of MILK secretion in either SEX, not necessarily related to PREGNANCY.
Alternative IDs:
ParentIDs:	MESH:D001941\|MESH:D011644
TreeNumbers:	C13.703.844.506 \|C17.800.090.937
Synonyms:	Disorder, Lactation \|Disorders, Lactation \|Hypogalactia \|Hypogalactias \|Lactation Disorder
Slim Mappings:	Pregnancy complication\|Skin disease
Reference:	MedGen: D007775 MeSH: D007775 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants