C8orf37-AS1, C8orf37 antisense RNA 1, 100616530

N. diseases: 12; N. variants: 18
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: C0018810
Disease: heart rate
heart rate 		phenotype Clinical Attribute 36 103 0.100 None 1.000 2 2 2018 2019
CUI: C0005890
Disease: Body Height
Body Height 		phenotype Organism Attribute 1903 3972 0.100 None 1.000 1 1 2019 2019
CUI: C4022792
Disease: Reduced ejection fraction
Reduced ejection fraction 		phenotype Finding 18 30 0.100 None 1.000 1 2 2019 2019
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 1074 306 0.100 None 1.000 1 1 2012 2012
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		phenotype Behavior and Behavior Mechanisms Individual Behavior 249 742 0.100 None 1.000 1 1 2015 2015
CUI: C0037369
Disease: Smoking
Smoking 		phenotype Behavior and Behavior Mechanisms Individual Behavior 391 765 0.100 None 1.000 1 1 2015 2015
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		disease Neoplasms Neoplastic Process 3111 6892 0.100 None 1.000 1 3 2017 2017
CUI: C0018801
Disease: Heart failure
Heart failure 		disease Cardiovascular Diseases Disease or Syndrome 1499 201 0.100 None 1.000 1 2 2019 2019
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 546 541 0.100 None 0 2
CUI: C3281045
Disease: CONE-ROD DYSTROPHY 16
CONE-ROD DYSTROPHY 16 		disease Disease or Syndrome 2 4 0.100 None 0 4
CUI: C3281046
Disease: RETINITIS PIGMENTOSA 64
RETINITIS PIGMENTOSA 64 		disease Disease or Syndrome 2 4 0.100 None 0 4
CUI: C4319932
Disease: BARDET-BIEDL SYNDROME 21
BARDET-BIEDL SYNDROME 21 		disease Disease or Syndrome 2 2 0.100 None 0 2