MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.080 None 1.000 8 2009 2020
CUI: C0854078
Disease: Diabetic end stage renal disease
Diabetic end stage renal disease
disease Disease or Syndrome 7 1 0.040 None 1.000 4 2010 2012
CUI: C0277792
Disease: Pathognomonic sign
Pathognomonic sign
phenotype Sign or Symptom 2 0.020 None 0.500 2 2010 2015
Cleft Lip with or without Cleft Palate
disease Congenital Abnormality 99 50 0.020 None 1.000 2 2009 2010
Finding of Mean Corpuscular Hemoglobin
phenotype Finding 653 1206 0.100 None 1.000 2 1 2016 2019
Human immunodeficiency virus (HIV) II infection category B1
disease Disease or Syndrome 985 56 0.020 None 1.000 2 2009 2010
CUI: C0005890
Disease: Body Height
Body Height
phenotype Organism Attribute 1903 3972 0.100 None 1.000 1 1 2019 2019
CUI: C0085662
Disease: Macrocytosis
Macrocytosis
disease Disease or Syndrome 13 0.010 None 1.000 1 2006 2006
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
phenotype Laboratory or Test Result 269 549 0.100 None 1.000 1 1 2016 2016
CUI: C0562350
Disease: Hip circumference
Hip circumference
phenotype Clinical Attribute 68 116 0.100 None 1.000 1 1 2018 2018
CUI: C0848765
Disease: Hearing disability
Hearing disability
disease Disease or Syndrome 6 2 0.010 None 1.000 1 1 2010 2010
CUI: C1285654
Disease: Memory performance
Memory performance
phenotype Mental Process 40 71 0.100 None 1.000 1 1 2017 2017
CUI: C1305904
Disease: Familial hematuria
Familial hematuria
disease Disease or Syndrome 23 7 0.010 None 1.000 1 1 2013 2013
CUI: C2749515
Disease: Collapsing glomerulopathy
Collapsing glomerulopathy
disease Disease or Syndrome 10 0.010 None 1.000 1 2010 2010
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 1 2018 2018
CUI: C4280711
Disease: Leukocyte inclusion bodies
Leukocyte inclusion bodies
phenotype Finding 1 0.400 strong 1.000 1 2012 2012
CUI: C4531083
Disease: Mucinous gastric carcinoma
Mucinous gastric carcinoma
disease Neoplastic Process 15 0.010 None 1.000 1 2016 2016
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time
phenotype Finding 39 3 0.100 None 0
Giant platelet (morphologic abnormality)
phenotype Finding 10 0.100 None 0
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies
phenotype Finding 271 106 0.100 None 0 1
CUI: C0855740
Disease: Abnormal platelet function
Abnormal platelet function
phenotype Finding 21 2 0.100 None 0 1
CUI: C0855742
Disease: Abnormal platelet morphology
Abnormal platelet morphology
phenotype Finding 10 1 0.100 None 0 1
CUI: C1096367
Disease: Increased mean platelet volume
Increased mean platelet volume
phenotype Finding 10 2 0.100 None 0 1
CUI: C1842774
Disease: Hypermelanotic macule
Hypermelanotic macule
phenotype Finding 59 2 0.100 None 0 1
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase
phenotype Finding 212 9 0.100 None 0