GNRH1, gonadotropin releasing hormone 1, 2796

N. diseases: 179; N. variants: 2
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: C1856897
Disease: Eunuchoidism, familial hypogonadotropic
Eunuchoidism, familial hypogonadotropic 		disease Endocrine System Diseases Disease or Syndrome 1 1 0.900 None 1.000 5 1 1977 2013
CUI: C4072887
Disease: Decreased circulating gonadotropin level
Decreased circulating gonadotropin level 		phenotype Finding 2 0.100 None 0
CUI: C1859391
Disease: Absent pubic hair
Absent pubic hair 		phenotype Finding 3 1 0.100 None 0
CUI: C0028838
Disease: Ocular Headache
Ocular Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2003 2003
CUI: C0423618
Disease: Throbbing Headache
Throbbing Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2003 2003
CUI: C0423623
Disease: Bilateral Headache
Bilateral Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2003 2003
CUI: C0474366
Disease: Generalized Headache
Generalized Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2003 2003
CUI: C0751187
Disease: Periorbital Headache
Periorbital Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2003 2003
CUI: C0751189
Disease: Retro-Ocular Headache
Retro-Ocular Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2003 2003
CUI: C0751190
Disease: Sharp Headache
Sharp Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2003 2003
CUI: C0751192
Disease: Vertex Headache
Vertex Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.300 None 1.000 1 2003 2003
CUI: C0877781
Disease: Hemicrania
Hemicrania 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 1 0.300 None 1.000 1 2003 2003
CUI: C0270749
Disease: Marie Cerebellar Ataxia
Marie Cerebellar Ataxia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 6 0.010 None 1.000 1 1982 1982
CUI: C0751186
Disease: Orthostatic Headache
Orthostatic Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 7 0.300 None 1.000 1 2003 2003
CUI: C0221405
Disease: Pituitary cachexia
Pituitary cachexia 		disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 8 0.200 None 1.000 2 1977 2009
CUI: C0271577
Disease: Isolated gonadotropin deficiency
Isolated gonadotropin deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 8 0.200 None 1.000 2 1977 2009
CUI: C2874188
Disease: Isolated deficiency of pituitary hormone
Isolated deficiency of pituitary hormone 		disease Disease or Syndrome 8 0.200 None 1.000 2 1977 2009
CUI: C2874189
Disease: Necrosis of pituitary gland (postpartum)
Necrosis of pituitary gland (postpartum) 		phenotype Pathologic Function 8 0.200 None 1.000 2 1977 2009
CUI: C2874190
Disease: Pituitary short stature
Pituitary short stature 		disease Disease or Syndrome 8 0.200 None 1.000 2 1977 2009
CUI: C0025319
Disease: Menopausal syndrome
Menopausal syndrome 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 8 0.010 None 1.000 1 2019 2019
CUI: C1859305
Disease: Cerebellar Ataxia and Hypogonadotropic Hypogonadism
Cerebellar Ataxia and Hypogonadotropic Hypogonadism 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 8 8 0.010 None 1.000 1 1982 1982
CUI: C0271582
Disease: Isolated lutropin deficiency (disorder)
Isolated lutropin deficiency (disorder) 		disease Endocrine System Diseases Disease or Syndrome 9 6 0.200 None 1.000 2 1977 2009
CUI: C0848255
Disease: female puberty
female puberty 		phenotype Sign or Symptom 9 0.010 None 1.000 1 2019 2019
CUI: C0342381
Disease: Idiopathic growth hormone deficiency
Idiopathic growth hormone deficiency 		disease Disease or Syndrome 10 0.200 None 1.000 2 1977 2009
CUI: C0751230
Disease: Hypothalamic Dysfunction Syndromes
Hypothalamic Dysfunction Syndromes 		disease Nervous System Diseases Disease or Syndrome 12 0.010 None 1.000 1 1992 1992