AIF1, allograft inflammatory factor 1, 199

N. diseases: 166; N. variants: 8
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: C0175693
Disease: Russell-Silver syndrome
Russell-Silver syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 104 12 0.010 None 1.000 1 2019 2019
CUI: C0178417
Disease: Anhedonia
Anhedonia
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 93 7 0.010 None 1.000 1 2018 2018
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
phenotype Pathological Conditions, Signs and Symptoms Neoplastic Process 3865 72 0.010 None 1.000 1 2017 2017
CUI: C0206019
Disease: HIV Encephalopathy
HIV Encephalopathy
disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 45 0.010 None 1.000 1 2016 2016
CUI: C0600041
Disease: Infective cystitis
Infective cystitis
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 106 0.010 None 1.000 1 2019 2019
CUI: C0678356
Disease: alcohol effect
alcohol effect
phenotype Disease or Syndrome 13 0.010 None 1.000 1 2019 2019
CUI: C1852467
Disease: Creutzfeldt-Jakob Disease, Sporadic
Creutzfeldt-Jakob Disease, Sporadic
disease Infections; Nervous System Diseases; Mental Disorders Disease or Syndrome 57 23 0.010 None 1.000 1 2003 2003
CUI: C1960443
Disease: Vasculitic neuropathy
Vasculitic neuropathy
disease Disease or Syndrome 13 0.010 None 1.000 1 2011 2011
CUI: C2747816
Disease: Complicated malaria
Complicated malaria
disease Infections Disease or Syndrome 166 38 0.010 None 1.000 1 2009 2009
CUI: C2900450
Disease: Other Creutzfeldt-Jakob disease
Other Creutzfeldt-Jakob disease
disease Infections; Nervous System Diseases; Mental Disorders Disease or Syndrome 37 18 0.010 None 1.000 1 2003 2003
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 123 10 0.010 None 1.000 1 2016 2016
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
group Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 2492 85 0.010 None 1.000 1 2012 2012
CUI: C2945695
Disease: Limb ischemia
Limb ischemia
disease Disease or Syndrome 171 3 0.010 None 1.000 1 2010 2010
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 254 51 0.010 None 1.000 1 2019 2019
Hereditary Diffuse Leukoencephalopathy with Spheroids
disease Nervous System Diseases Disease or Syndrome 9 44 0.010 None 1.000 1 2016 2016
CUI: C3887524
Disease: Skin Erosion
Skin Erosion
disease Skin and Connective Tissue Diseases Disease or Syndrome 225 2 0.010 None 1.000 1 2016 2016
CUI: C3899658
Disease: Childhood Gliosarcoma
Childhood Gliosarcoma
disease Neoplasms Neoplastic Process 44 5 0.010 None 1.000 1 2000 2000
CUI: C4048328
Disease: cervical cancer
cervical cancer
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 1817 268 0.010 None < 0.001 1 2014 2014
CUI: C4049883
Disease: Obstructive Ureterocele
Obstructive Ureterocele
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 25 0.010 None 1.000 1 2012 2012
SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 36 19 0.010 None 1.000 1 2018 2018
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 110 29 0.010 None 1.000 1 2013 2013
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 3720 652 0.010 None 1.000 1 2014 2014
CUI: C4479709
Disease: FCD IIB
FCD IIB
disease Disease or Syndrome 15 2 0.010 None 1.000 1 2018 2018
MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 32 8 0.010 None 1.000 1 2019 2019
CUI: C0878486
Disease: Arteriolosclerosis
Arteriolosclerosis
disease Cardiovascular Diseases Disease or Syndrome 13 2 0.010 None 1.000 1 2016 2016