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: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency 		disease Disease or Syndrome 168 27 0.010 None 1.000 1 1986 1986
CUI: C0020514
Disease: Hyperprolactinemia
Hyperprolactinemia 		disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 48 10 0.300 None 1.000 1 1990 1990
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		group Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 2780 385 0.010 None 1.000 1 1991 1991
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 919 110 0.010 None 1.000 1 1992 1992
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 254 56 0.010 None 1.000 1 1992 1992
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
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1182 189 0.010 None 1.000 1 1992 1992
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency 		disease Disease or Syndrome 55 28 0.010 None 1.000 1 1993 1993
CUI: C0268287
Disease: Deficiency of steroid 21-monooxygenase
Deficiency of steroid 21-monooxygenase 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 54 26 0.010 None 1.000 1 1993 1993
CUI: C2936858
Disease: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 50 62 0.010 None 1.000 1 1993 1993
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.010 None 1.000 1 1993 1993
CUI: C0747102
Disease: Ovarian failure
Ovarian failure 		disease Endocrine System Diseases Disease or Syndrome 39 1 0.020 None 0.500 2 1990 1996
CUI: C1853926
Disease: NONAKA MYOPATHY
NONAKA MYOPATHY 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 132 81 0.010 None 1.000 1 2001 2001
CUI: C0002793
Disease: Anaplasia
Anaplasia 		disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 538 7 0.010 None 1.000 1 2001 2001
CUI: C1328504
Disease: Hormone refractory prostate cancer
Hormone refractory prostate cancer 		disease Neoplasms; Male Urogenital Diseases Neoplastic Process 683 29 0.010 None 1.000 1 2001 2001
CUI: C1514428
Disease: Primary peritoneal carcinoma
Primary peritoneal carcinoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 49 0.010 None 1.000 1 2001 2001
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: 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: 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: C1840311
Disease: Laryngeal cleft
Laryngeal cleft 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 72 4 0.010 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: C1527358
Disease: Phototoxicity
Phototoxicity 		disease Skin and Connective Tissue Diseases Disease or Syndrome 52 0.010 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: 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: C0751186
Disease: Orthostatic Headache
Orthostatic Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 7 0.300 None 1.000 1 2003 2003