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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: Hyperpituitarism (D006964)
..Starting node ..Hyperprolactinemia (D006966)
Child Nodes:
........Galactorrhea-Hyperprolactinemia (C535402)
Sister Nodes:
..Acromegaly (D000172) 6
..Gigantism (D005877) 1
..Hyperprolactinemia (D006966) 1
..Pituitary ACTH Hypersecretion (D047748) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5470
Name:	Hyperprolactinemia
Definition:	Increased levels of PROLACTIN in the BLOOD, which may be associated with AMENORRHEA and GALACTORRHEA. Relatively common etiologies include PROLACTINOMA, medication effect, KIDNEY FAILURE, granulomatous diseases of the PITUITARY GLAND, and disorders which interfere with the hypothalamic inhibition of prolactin release. Ectopic (non-pituitary) production of prolactin may also occur. (From Joynt, Clinical Neurology, 1992, Ch36, pp77-8)
Alternative IDs:
ParentIDs:	MESH:D006964
TreeNumbers:	C10.228.140.617.738.250.450 \|C19.700.355.600
Synonyms:	Hyperprolactinaemia \|Hyperprolactinemias \|Hypersecretion Syndrome, Prolactin \|Inappropriate Prolactin Secretion \|Inappropriate Prolactin Secretion Syndrome \|Inappropriate Secretion Prolactin \|Prolactin Hypersecretion Syndrome \|Prolactin, Inappropriate Secretion
Slim Mappings:	Endocrine system disease\|Nervous system disease
Reference:	MedGen: D006966 MeSH: D006966 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants