LEPR, leptin receptor, 3953

N. diseases: 300; N. variants: 31
Source: BEFREE ×
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: C4316791
Disease: Entamoeba histolytica Infection
Entamoeba histolytica Infection 		disease Infections Disease or Syndrome 2 0.020 None 1.000 2 2011 2014
CUI: C3838754
Disease: Congenital leptin deficiency
Congenital leptin deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome; Congenital Abnormality 3 0.010 None 1.000 1 2018 2018
CUI: C1449647
Disease: Secondary Peritonitis
Secondary Peritonitis 		disease Digestive System Diseases; Infections Disease or Syndrome 5 0.010 None 1.000 1 2011 2011
CUI: C1997092
Disease: Hypertensive left ventricular hypertrophy
Hypertensive left ventricular hypertrophy 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 1 2013 2013
CUI: C3274639
Disease: Neonatal Opiate Withdrawal Syndrome
Neonatal Opiate Withdrawal Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Mental or Behavioral Dysfunction 6 0.010 None 1.000 1 2019 2019
CUI: C3554225
Disease: LEPTIN RECEPTOR DEFICIENCY
LEPTIN RECEPTOR DEFICIENCY 		disease Disease or Syndrome 9 0.720 strong 1.000 2 1998 2019
CUI: C1504375
Disease: Diabetic macroangiopathy
Diabetic macroangiopathy 		disease Disease or Syndrome 9 2 0.010 None 1.000 1 2012 2012
CUI: C4505163
Disease: Food Addiction
Food Addiction 		disease Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 9 3 0.010 None 1.000 1 2013 2013
CUI: C0948368
Disease: Kaufman-McKusick syndrome
Kaufman-McKusick syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 10 2 0.010 None 1.000 1 2011 2011
CUI: C4054476
Disease: Monogenic Obesity
Monogenic Obesity 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Sign or Symptom 11 1 0.030 None 1.000 3 2003 2018
CUI: C0405581
Disease: Testicular dysfunction
Testicular dysfunction 		disease Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 13 0.010 None 1.000 1 2018 2018
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		disease Disease or Syndrome 15 0.040 None 1.000 4 2018 2019
CUI: C0342538
Disease: Constitutional delay of growth and puberty
Constitutional delay of growth and puberty 		disease Disease or Syndrome 16 7 0.010 None < 0.001 1 2006 2006
CUI: C1845118
Disease: SHORT STATURE, IDIOPATHIC, X-LINKED
SHORT STATURE, IDIOPATHIC, X-LINKED 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 18 2 0.010 None 1.000 1 1 2012 2012
CUI: C4700045
Disease: Non-ST-segment elevation myocardial infarction (NSTEMI)
Non-ST-segment elevation myocardial infarction (NSTEMI) 		disease Disease or Syndrome 18 1 0.010 None 1.000 1 1 2018 2018
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism 		disease Endocrine System Diseases Disease or Syndrome 19 1 0.010 None 1.000 1 2018 2018
CUI: C1260965
Disease: Lipoblastoma
Lipoblastoma 		disease Neoplasms Neoplastic Process 20 0.010 None 1.000 1 1999 1999
CUI: C1504532
Disease: Post transplant diabetes mellitus
Post transplant diabetes mellitus 		disease Disease or Syndrome 21 11 0.010 None 1.000 1 1 2019 2019
CUI: C0948242
Disease: Nuchal bleb, familial
Nuchal bleb, familial 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Congenital Abnormality 23 9 0.010 None 1.000 1 1 2006 2006
CUI: C0011848
Disease: Diabetes Insipidus
Diabetes Insipidus 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 26 0.010 None 1.000 1 2006 2006
CUI: C0271801
Disease: Central hypothyroidism
Central hypothyroidism 		disease Endocrine System Diseases Disease or Syndrome 27 0.010 None 1.000 1 2001 2001
CUI: C0342543
Disease: Central Precocious Puberty
Central Precocious Puberty 		disease Endocrine System Diseases Disease or Syndrome 27 2 0.010 None 1.000 1 2012 2012
CUI: C0023886
Disease: Liver Abscess, Amebic
Liver Abscess, Amebic 		disease Digestive System Diseases; Infections Disease or Syndrome 30 1 0.010 None 1.000 1 1 2014 2014
CUI: C0205825
Disease: Liposarcoma, Pleomorphic
Liposarcoma, Pleomorphic 		disease Neoplasms Neoplastic Process 31 0.010 None 1.000 1 2001 2001
CUI: C1096293
Disease: Macroangiopathy
Macroangiopathy 		disease Disease or Syndrome 31 6 0.010 None 1.000 1 2012 2012