PRL, prolactin, 5617

N. diseases: 506; N. variants: 3
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0005001
Disease: Benign prostatic hypertrophy
Benign prostatic hypertrophy 		phenotype Male Urogenital Diseases Pathologic Function 4 0.300 None 1.000 1 1990 1990
CUI: C0008909
Disease: Claustrophobia
Claustrophobia 		phenotype Mental Disorders Mental or Behavioral Dysfunction 4 0.300 None 1.000 1 1989 1989
CUI: C0014008
Disease: Empty Sella Syndrome
Empty Sella Syndrome 		disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C0020610
Disease: Hypogalactia
Hypogalactia 		disease Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
CUI: C0032963
Disease: Pregnancy Complications, Cardiovascular
Pregnancy Complications, Cardiovascular 		disease Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Disease or Syndrome 4 0.300 None 1.000 1 2008 2008
CUI: C0235969
Disease: Disorder of ejaculation
Disorder of ejaculation 		disease Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0473315
Disease: Lactational amenorrhea
Lactational amenorrhea 		disease Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C2673535
Disease: DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)
DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder) 		disease Nervous System Diseases Disease or Syndrome 4 56 0.010 None 1.000 1 2017 2017
CUI: C0269972
Disease: Postpartum cardiomyopathy
Postpartum cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 5 0.010 None 1.000 1 2007 2007
CUI: C0346304
Disease: Gonadotroph adenoma
Gonadotroph adenoma 		disease Neoplasms; Nervous System Diseases; Endocrine System Diseases Neoplastic Process 5 0.010 None 1.000 1 1991 1991
CUI: C0858734
Disease: Insulin hypoglycemia
Insulin hypoglycemia 		disease Disease or Syndrome 5 0.010 None 1.000 1 1990 1990
CUI: C0878676
Disease: 6-pyruvoyl-tetrahydropterin synthase deficiency
6-pyruvoyl-tetrahydropterin synthase deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 5 38 0.010 None 1.000 1 2008 2008
CUI: C0016722
Disease: Frigidity
Frigidity 		disease Mental Disorders Mental or Behavioral Dysfunction 6 0.300 None 1.000 2 1997 2005
CUI: C0029261
Disease: Orgasmic Disorder
Orgasmic Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 6 0.300 None 1.000 2 1997 2005
CUI: C0033953
Disease: Psychosexual Disorders
Psychosexual Disorders 		group Mental Disorders Mental or Behavioral Dysfunction 6 0.300 None 1.000 2 1997 2005
CUI: C0018050
Disease: Gonadal Disorders
Gonadal Disorders 		group Endocrine System Diseases Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C0032796
Disease: Postpartum Amenorrhea
Postpartum Amenorrhea 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 6 0.300 None 1.000 1 1980 1980
CUI: C0553573
Disease: Primary infertility
Primary infertility 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 6 2 0.010 None 1.000 1 2015 2015
CUI: C3665358
Disease: Galactorrhea
Galactorrhea 		disease Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases Finding 6 0.300 None 1.000 1 2010 2010
CUI: C0020594
Disease: Hypoactive Sexual Desire Disorder
Hypoactive Sexual Desire Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 7 0.300 None 1.000 2 1997 2005
CUI: C0036902
Disease: Sexual Arousal Disorder
Sexual Arousal Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 7 0.300 None 1.000 2 1997 2005
CUI: C3203671
Disease: CYP2D6 polymorphism
CYP2D6 polymorphism 		disease Disease or Syndrome 7 5 0.010 None 1.000 1 2007 2007
CUI: C4302200
Disease: Congenital central hypothyroidism
Congenital central hypothyroidism 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 8 0.020 None 1.000 2 2013 2018
CUI: C0015951
Disease: Fetal Resorption
Fetal Resorption 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 8 0.300 None 1.000 1 1986 1986
CUI: C0520477
Disease: Prostatic Adenoma
Prostatic Adenoma 		disease Male Urogenital Diseases Neoplastic Process 8 0.300 None 1.000 1 1990 1990