RPS19, ribosomal protein S19, 6223

N. diseases: 256; N. variants: 17
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: C0272170
Disease: Shwachman syndrome
Shwachman syndrome 		disease Disease or Syndrome 49 13 0.100 None 1.000 12 2006 2019
CUI: C0542035
Disease: Erythroid hypoplasia
Erythroid hypoplasia 		disease Disease or Syndrome 14 1 0.070 None 0.857 7 1999 2019
CUI: C0877221
Disease: Decreased erythroid precursor production
Decreased erythroid precursor production 		disease Disease or Syndrome 3 0.070 None 0.857 7 1999 2019
CUI: C0000846
Disease: Agenesis
Agenesis 		disease Congenital Abnormality 161 44 0.030 None 1.000 3 1996 1997
CUI: C0740997
Disease: Anemia, normochromic macrocytic
Anemia, normochromic macrocytic 		disease Disease or Syndrome 1 0.030 None 1.000 3 2000 2019
CUI: C0026985
Disease: Myelodysplasia
Myelodysplasia 		disease Congenital Abnormality 181 4 0.120 None 1.000 2 2018 2019
CUI: C0241391
Disease: Thumb absent
Thumb absent 		phenotype Finding 21 0.400 strong 1.000 2 1991 2004
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.020 None 1.000 2 2012 2018
CUI: C2062441
Disease: Influenza A
Influenza A 		disease Disease or Syndrome 563 19 0.020 None 1.000 2 2017 2018
CUI: C2751481
Disease: Mild radial hypoplasia
Mild radial hypoplasia 		phenotype Finding 1 0.300 strong 1.000 2 1991 2004
CUI: C2931245
Disease: Bone Marrow failure syndromes
Bone Marrow failure syndromes 		disease Disease or Syndrome 41 0.020 None 1.000 2 2006 2018
CUI: C0085662
Disease: Macrocytosis
Macrocytosis 		disease Disease or Syndrome 13 0.010 None 1.000 1 1999 1999
CUI: C0220810
Disease: Congenital defects
Congenital defects 		group Congenital Abnormality 126 6 0.010 None 1.000 1 2018 2018
CUI: C0231706
Disease: Circling gait
Circling gait 		phenotype Sign or Symptom 9 1 0.010 None 1.000 1 2019 2019
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders 		group Mental or Behavioral Dysfunction 360 56 0.010 None 1.000 1 2019 2019
CUI: C0238790
Disease: bone destruction
bone destruction 		disease Disease or Syndrome 234 3 0.010 None 1.000 1 2005 2005
CUI: C0272138
Disease: Erythroblastosis
Erythroblastosis 		disease Disease or Syndrome 89 0.010 None 1.000 1 2018 2018
CUI: C0334070
Disease: Maturation defect
Maturation defect 		phenotype Acquired Abnormality 43 2 0.010 None 1.000 1 1999 1999
CUI: C0427032
Disease: Ankle stiff
Ankle stiff 		phenotype Sign or Symptom 2 0.010 None 1.000 1 2020 2020
CUI: C0683357
Disease: Excessive drinking
Excessive drinking 		phenotype Mental or Behavioral Dysfunction 15 1 0.010 None 1.000 1 2017 2017
CUI: C0683381
Disease: inflammatory joint disease
inflammatory joint disease 		disease Disease or Syndrome 33 0.010 None 1.000 1 2017 2017
CUI: C0741237
Disease: arthritis symptoms
arthritis symptoms 		disease Disease or Syndrome 9 0.010 None 1.000 1 2015 2015
CUI: C0741949
Disease: Cardiovascular Pathology
Cardiovascular Pathology 		disease Disease or Syndrome 23 0.010 None 1.000 1 2017 2017
CUI: C1536075
Disease: Sudden unexplained death in epilepsy
Sudden unexplained death in epilepsy 		disease Disease or Syndrome 12 0.010 None 1.000 1 2019 2019
CUI: C1542667
Disease: Congenital erythroid hypoplasia
Congenital erythroid hypoplasia 		disease Congenital Abnormality 3 0.010 None 1.000 1 2017 2017