Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1850406
Disease: NAVAJO NEUROHEPATOPATHY
NAVAJO NEUROHEPATOPATHY
0.760 Biomarker disease CTD_human
CUI: C1850406
Disease: NAVAJO NEUROHEPATOPATHY
NAVAJO NEUROHEPATOPATHY
0.760 Biomarker disease GENOMICS_ENGLAND
CUI: C0013421
Disease: Dystonia
Dystonia
0.400 Biomarker phenotype GENOMICS_ENGLAND
CUI: C0013421
Disease: Dystonia
Dystonia
0.400 Biomarker phenotype HPO
CUI: C0344307
Disease: Absence of pain sensation
Absence of pain sensation
0.400 Biomarker phenotype HPO
Navajo Familial Neurogenic Arthropathy
0.300 Biomarker disease CTD_human
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
0.220 Biomarker group MGD
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
0.120 Biomarker disease HPO
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
0.110 Biomarker disease HPO
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
0.100 Biomarker phenotype HPO
CUI: C0003079
Disease: Anisocoria
Anisocoria
0.100 CausalMutation phenotype CLINVAR
CUI: C0003079
Disease: Anisocoria
Anisocoria
0.100 GeneticVariation phenotype CLINVAR
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 Biomarker phenotype HPO
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0.100 GeneticVariation disease CLINVAR
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0.100 CausalMutation disease CLINVAR
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.100 Biomarker phenotype HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.100 Biomarker disease HPO
CUI: C0018681
Disease: Headache
Headache
0.100 GeneticVariation phenotype CLINVAR
CUI: C0018681
Disease: Headache
Headache
0.100 CausalMutation phenotype CLINVAR
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
0.100 Biomarker phenotype HPO
CUI: C0020580
Disease: Hypesthesia
Hypesthesia
0.100 GeneticVariation phenotype CLINVAR
CUI: C0020580
Disease: Hypesthesia
Hypesthesia
0.100 CausalMutation phenotype CLINVAR
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia
0.100 Biomarker disease HPO
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.100 Biomarker disease HPO
CUI: C0030196
Disease: Pain in limb
Pain in limb
0.100 CausalMutation phenotype CLINVAR