RSRP1, arginine and serine rich protein 1, 57035

N. diseases: 13; 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: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Experimental Model of Disease 870 0.300 None 1.000 1 2014 2014
Red cell distribution width determination
phenotype Laboratory Procedure 593 988 0.100 None 1.000 2 2 2016 2019
RDW - Red blood cell distribution width result
phenotype Laboratory or Test Result 593 988 0.100 None 1.000 2 2 2016 2019
CUI: C0005833
Disease: Blood Sedimentation
Blood Sedimentation
phenotype Laboratory Procedure 7 8 0.100 None 1.000 1 1 2011 2011
Anti-D isoimmunization affecting pregnancy
disease Disease or Syndrome 2 1 0.100 None 1.000 1 1 2017 2017
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 1 2018 2018
erythrocyte sedimentation rate result
phenotype Laboratory or Test Result 5 5 0.100 None 1.000 1 1 2011 2011
Finding of Mean Corpuscular Hemoglobin
phenotype Finding 653 1206 0.100 None 1.000 1 1 2019 2019
Hemolytic disease of fetus OR newborn due to RhD isoimmunization
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 3 1 0.100 None 1.000 1 1 2017 2017
Corpuscular Hemoglobin Concentration Mean
phenotype Laboratory or Test Result 401 4389 0.100 None 1.000 1 1 2016 2016
CUI: C4015919
Disease: RHD CATEGORY D-VII
RHD CATEGORY D-VII
phenotype Finding 2 1 0.100 None 0 1
CUI: C4015920
Disease: RHD, WEAK D, TYPE I
RHD, WEAK D, TYPE I
phenotype Finding 2 1 0.100 None 0 1
CUI: C4023620
Disease: Blood group antigen abnormality
Blood group antigen abnormality
phenotype Anatomical Abnormality 8 6 0.100 None 0 1