IFNG, interferon gamma, 3458

N. diseases: 1519; 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: C0858867
Disease: Reticulocytopenia
Reticulocytopenia
phenotype Finding 17 0.100 None 0
CUI: C1332852
Disease: Cardiac rhabdomyoma
Cardiac rhabdomyoma
disease Neoplasms; Cardiovascular Diseases Neoplastic Process 6 1 0.100 None 0
Localized Primitive Neuroectodermal Tumor
disease Neoplasms Neoplastic Process 4 0.200 None 0
MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)
disease Finding 10 3 0.300 None 0
CUI: C1855710
Disease: Bone marrow hypocellularity
Bone marrow hypocellularity
phenotype Finding 64 5 0.100 None 0
CUI: C1860707
Disease: TUBEROUS SCLEROSIS 2 (disorder)
TUBEROUS SCLEROSIS 2 (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases Disease or Syndrome 43 255 0.300 None 0
CUI: C1860710
Disease: Achromatic retinal patches
Achromatic retinal patches
phenotype Finding 3 0.100 None 0
CUI: C1968958
Disease: Subependymal nodules
Subependymal nodules
phenotype Finding 3 1 0.100 None 0
CUI: C1968959
Disease: Cortical tubers
Cortical tubers
phenotype Finding 3 4 0.100 None 0
APLASTIC ANEMIA, SUSCEPTIBILITY TO (finding)
disease Finding 3 2 0.100 None 0 1
Tsc2 Angiomyolipomas, Renal, Modifier Of
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases Disease or Syndrome 2 1 0.100 None 0 1
CUI: C3887499
Disease: Renal cyst
Renal cyst
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 170 17 0.100 None 0
CUI: C4025790
Disease: Specific learning disability
Specific learning disability
disease Mental or Behavioral Dysfunction 165 13 0.100 None 0
CUI: C0020625
Disease: Hyponatremia
Hyponatremia
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 109 11 0.300 None 1.000 1 1986 1986
CUI: C0020649
Disease: Hypotension
Hypotension
phenotype Cardiovascular Diseases Finding 125 2 0.300 None 1.000 1 1986 1986
CUI: C0027497
Disease: Nausea
Nausea
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 161 14 0.300 None 1.000 1 1986 1986
CUI: C0042963
Disease: Vomiting
Vomiting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 303 23 0.300 None 1.000 1 1986 1986
CUI: C0085593
Disease: Chills
Chills
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 34 0.300 None 1.000 1 1986 1986
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 546 541 0.010 None 1.000 1 1987 1987
CUI: C0702159
Disease: Constitutional aplastic anemia
Constitutional aplastic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 5 0.010 None 1.000 1 1988 1988
CUI: C0020951
Disease: Immune Complex Diseases
Immune Complex Diseases
group Immune System Diseases Disease or Syndrome 10 0.300 None 1.000 1 1991 1991
CUI: C1704377
Disease: Bright Disease
Bright Disease
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 31 0.300 None 1.000 1 1991 1991
CUI: C3899403
Disease: Decreased Concentration
Decreased Concentration
phenotype Sign or Symptom 27 1 0.010 None 1.000 1 1991 1991
CUI: C0002893
Disease: Refractory anemias
Refractory anemias
disease Hemic and Lymphatic Diseases Disease or Syndrome 340 11 0.010 None 1.000 1 1 1992 1992
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 664 22 0.010 None 1.000 1 1992 1992