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.
Autosomal dominant retinitis pigmentosa
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 85 65 0.100 None 1.000 17 11 1995 2013
CUI: C1867299
Disease: Retinitis Pigmentosa 10
Retinitis Pigmentosa 10
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 3 8 0.720 None 1.000 5 7 2002 2008
Amaurosis congenita of Leber, type 1
disease Eye Diseases Disease or Syndrome 81 60 0.020 None 1.000 2 1 2006 2006
CUI: C1998028
Disease: Photoreceptor degeneration
Photoreceptor degeneration
disease Eye Diseases Disease or Syndrome 136 16 0.020 None 1.000 2 2006 2010
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
group Eye Diseases Disease or Syndrome 714 56 0.020 None 0.500 2 2006 2008
Phosphoglycerate Kinase 1 Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 18 0.010 None 1.000 1 4 2006 2006
CUI: C0867389
Disease: Chronic graft-versus-host disease
Chronic graft-versus-host disease
disease Immune System Diseases Disease or Syndrome 241 17 0.010 None 1.000 1 1 2018 2018
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration
phenotype Eye Diseases Pathologic Function 125 2 0.010 None 1.000 1 2005 2005
CUI: C1842475
Disease: Retinitis Pigmentosa 7
Retinitis Pigmentosa 7
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 7 22 0.010 None 1.000 1 1996 1996
CUI: C0220701
Disease: RETINITIS PIGMENTOSA 1
RETINITIS PIGMENTOSA 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 32 21 0.010 None 1.000 1 2008 2008
CUI: C1840284
Disease: LEBER CONGENITAL AMAUROSIS 11
LEBER CONGENITAL AMAUROSIS 11
disease Eye Diseases Disease or Syndrome 1 1 0.700 None 1.000 1 1 2006 2006
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
disease Eye Diseases Disease or Syndrome 685 663 0.010 None 1.000 1 2006 2006
CUI: C0948168
Disease: Bone marrow toxicity
Bone marrow toxicity
disease Disease or Syndrome 13 0.010 None 1.000 1 2010 2010
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
disease Immune System Diseases Disease or Syndrome 294 49 0.010 None 1.000 1 2 2012 2012
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 6776 2793 0.010 None < 0.001 1 2012 2012
Deficiency of phosphoglycerate kinase
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 6 0.010 None 1.000 1 4 2006 2006
CUI: C0024437
Disease: Macular degeneration
Macular degeneration
disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 44 16 0.010 None 1.000 1 2006 2006
CUI: C0024312
Disease: Lymphopenia
Lymphopenia
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 239 16 0.010 None 1.000 1 1 2015 2015
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 6941 3417 0.010 None < 0.001 1 2012 2012
CUI: C0011847
Disease: Diabetes
Diabetes
disease Endocrine System Diseases Disease or Syndrome 2359 710 0.010 None 1.000 1 2013 2013
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
group Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 2803 824 0.010 None 1.000 1 2013 2013
CUI: C0456909
Disease: Blindness
Blindness
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 393 34 0.110 None 1.000 1 2006 2006
CUI: C0005754
Disease: Congenital blindness
Congenital blindness
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Nervous System Diseases Congenital Abnormality 16 3 0.010 None 1.000 1 2010 2010
Congenital Amaurosis of Retinal Origin
disease Eye Diseases Disease or Syndrome 8 0.300 None 1.000 1 2006 2006
CUI: C0023530
Disease: Leukopenia
Leukopenia
disease Hemic and Lymphatic Diseases Disease or Syndrome 440 153 0.010 None 1.000 1 2 2017 2017