EFNA5, ephrin A5, 1946

N. diseases: 66; N. variants: 10
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: C0544852
Disease: Hypertrichosis, universal
Hypertrichosis, universal 		disease Disease or Syndrome 1 0.010 None 1.000 1 1998 1998
CUI: C1840362
Disease: HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE (disorder)
HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE (disorder) 		disease Skin and Connective Tissue Diseases Disease or Syndrome 2 0.010 None 1.000 1 1998 1998
CUI: C4554010
Disease: Isomerism (body)
Isomerism (body) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases Congenital Abnormality 9 0.010 None 1.000 1 2019 2019
CUI: C1862596
Disease: Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 12 24 0.010 None 1.000 1 1989 1989
CUI: C4315130
Disease: Hippocampal atrophy
Hippocampal atrophy 		phenotype Finding 13 12 0.100 None 1.000 1 1 2009 2009
CUI: C1533568
Disease: fertility disorders
fertility disorders 		group Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 18 0.010 None 1.000 1 2018 2018
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 20 11 0.010 None 1.000 1 1989 1989
CUI: C0149654
Disease: Conduct Disorder
Conduct Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 34 18 0.010 None 1.000 1 2004 2004
CUI: C0003838
Disease: Arterial Occlusive Diseases
Arterial Occlusive Diseases 		group Cardiovascular Diseases Disease or Syndrome 35 4 0.010 None 1.000 1 2002 2002
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		disease Eye Diseases Disease or Syndrome 42 3 0.010 None 1.000 1 2015 2015
CUI: C0002902
Disease: Anencephaly
Anencephaly 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 59 10 0.200 None 1.000 2 2000 2000
CUI: C0029182
Disease: orbit (eye disorders)
orbit (eye disorders) 		group Eye Diseases Disease or Syndrome 64 0.020 None 1.000 2 2017 2018
CUI: C0006370
Disease: Bulimia
Bulimia 		disease Pathological Conditions, Signs and Symptoms Mental or Behavioral Dysfunction 76 30 0.010 None 1.000 1 2018 2018
CUI: C0036646
Disease: Age-related cataract
Age-related cataract 		disease Eye Diseases Acquired Abnormality 92 15 0.010 None 1.000 1 2014 2014
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 94 48 0.010 None 1.000 1 2018 2018
CUI: C0001857
Disease: AIDS related complex
AIDS related complex 		disease Infections; Immune System Diseases Disease or Syndrome 100 43 0.010 None 1.000 1 3 2014 2014
CUI: C0038358
Disease: Gastric ulcer
Gastric ulcer 		disease Digestive System Diseases Disease or Syndrome 136 7 0.010 None 1.000 1 1992 1992
CUI: C0042798
Disease: Low Vision
Low Vision 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 157 51 0.010 None 1.000 1 2018 2018
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		phenotype Laboratory Procedure 160 355 0.100 None 1.000 1 1 2018 2018
CUI: C0521707
Disease: Bilateral cataracts (disorder)
Bilateral cataracts (disorder) 		disease Eye Diseases Disease or Syndrome 166 37 0.010 None 1.000 1 2017 2017
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 175 112 0.010 None 1.000 1 2018 2018
CUI: C0039103
Disease: Synovitis
Synovitis 		disease Musculoskeletal Diseases Disease or Syndrome 197 0.010 None 1.000 1 1992 1992
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		disease Nervous System Diseases Disease or Syndrome 241 69 0.010 None 1.000 1 2018 2018
CUI: C0035126
Disease: Reperfusion Injury
Reperfusion Injury 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Injury or Poisoning 300 0.300 None 1.000 1 2006 2006
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis 		phenotype Disease or Syndrome 328 0.010 None 1.000 1 2017 2017