Hyperprolactinemia (HPRL)

Alias:
Chiari-Frommel Syndrome
Hyperprolactinaemia
Familial Hyperprolactinemia
Hprl
Familial Isolated Prolactin Receptor Deficiency
Pregnancy-Related a-G Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hyperprolactinemia, also known as chiari-frommel syndrome, is related to galactorrhea and prolactinoma. An important gene associated with Hyperprolactinemia is PRLR (Prolactin Receptor), and among its related pathways/superpathways are Signal Transduction and GPCR downstream signalling. The drugs Quinagolide and Aripiprazole have been mentioned in the context of this disorder. Affiliated tissues include pituitary and ovary, and related phenotypes are galactorrhea and oligomenorrhea
Related ID:
MESH:D002640
ICD11:1417218455

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
--
25
264
8

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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