LHB, luteinizing hormone subunit beta, 3972

N. diseases: 62; N. variants: 11
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: C1858573
Disease: Sparse pubic hair
Sparse pubic hair
phenotype Finding 42 0.100 None 0
CUI: C0425957
Disease: Secondary amenorrhea
Secondary amenorrhea
phenotype Pathological Conditions, Signs and Symptoms Finding 49 0.100 None 0
CUI: C0029927
Disease: Ovarian Cysts
Ovarian Cysts
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Disease or Syndrome 74 3 0.100 None 0
CUI: C0028949
Disease: Oligomenorrhea
Oligomenorrhea
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 37 1 0.100 None 0
CUI: C0520933
Disease: Abnormal spermatogenesis
Abnormal spermatogenesis
phenotype Male Urogenital Diseases Finding 5 0.100 None 0
CUI: C4073137
Disease: Decreased serum testosterone level
Decreased serum testosterone level
phenotype Finding 47 0.100 None 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis
disease Male Urogenital Diseases Congenital Abnormality 217 11 0.100 None 0
CUI: C0232940
Disease: Secondary physiologic amenorrhea
Secondary physiologic amenorrhea
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 58 2 0.100 None 0
CUI: C1864873
Disease: Testicular Microlithiasis
Testicular Microlithiasis
disease Pathological Conditions, Signs and Symptoms; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 6 4 0.100 None 0
Deficiency of testosterone biosynthesis
disease Endocrine System Diseases Disease or Syndrome 18 0.100 None 0
Decreased circulating luteinizing hormone level
phenotype Finding 6 0.100 None 0
CUI: C4023703
Disease: Abnormality of the Leydig cells
Abnormality of the Leydig cells
disease Anatomical Abnormality 4 0.100 None 0
CUI: C0018418
Disease: Gynecomastia
Gynecomastia
disease Skin and Connective Tissue Diseases Disease or Syndrome 121 8 0.100 None 0
CUI: C1858574
Disease: Sparse axillary hair
Sparse axillary hair
phenotype Finding 39 0.100 None 0
Abnormality of metabolism/homeostasis
phenotype Finding 171 5 0.100 None 0
CUI: C0020514
Disease: Hyperprolactinemia
Hyperprolactinemia
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 48 10 0.300 None 1.000 1 1980 1980
CUI: C0039231
Disease: Tachycardia
Tachycardia
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Finding 73 8 0.300 None 1.000 1 1983 1983
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.300 None 1.000 1 1983 1983
CUI: C0428977
Disease: Bradycardia
Bradycardia
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Finding 63 2 0.300 None 1.000 1 1983 1983
CUI: C0080203
Disease: Tachyarrhythmia
Tachyarrhythmia
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Finding 18 0.300 None 1.000 1 1983 1983
CUI: C0020672
Disease: Hypothermia, natural
Hypothermia, natural
phenotype Pathological Conditions, Signs and Symptoms Finding 52 3 0.300 None 1.000 1 1983 1983
Isolated lutropin deficiency (disorder)
disease Endocrine System Diseases Disease or Syndrome 9 6 0.700 strong 1.000 1 5 1992 1992
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 218 54 0.300 None 1.000 1 1996 1996
CUI: C0085762
Disease: Alcohol abuse
Alcohol abuse
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 156 24 0.300 None 1.000 1 1996 1996
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 577 441 0.300 None 1.000 1 1996 1996