Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1865270
Disease: BARTTER SYNDROME, TYPE 4A
BARTTER SYNDROME, TYPE 4A
0.910 Biomarker disease CTD_human
CUI: C0004775
Disease: Bartter Disease
Bartter Disease
0.400 Biomarker disease GENOMICS_ENGLAND
Sensorineural Deafness With Mild Renal Dysfunction
0.300 CausalMutation disease CLINVAR
Sensorineural Hearing Loss (disorder)
0.200 Biomarker disease HPO
CUI: C0020428
Disease: Hyperaldosteronism
Hyperaldosteronism
0.110 Biomarker disease HPO
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency
0.110 Biomarker disease HPO
CUI: C0013604
Disease: Edema
Edema
0.100 Biomarker phenotype HPO
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
0.100 Biomarker disease HPO
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker phenotype HPO
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis
0.100 Biomarker disease HPO
CUI: C0020621
Disease: Hypokalemia
Hypokalemia
0.100 Biomarker phenotype HPO
CUI: C0020625
Disease: Hyponatremia
Hyponatremia
0.100 Biomarker phenotype HPO
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0.100 Biomarker phenotype HPO
CUI: C0032617
Disease: Polyuria
Polyuria
0.100 Biomarker phenotype HPO
CUI: C0085680
Disease: Hypochloremia (disorder)
Hypochloremia (disorder)
0.100 Biomarker disease HPO
CUI: C0151526
Disease: Premature Birth
Premature Birth
0.100 Biomarker phenotype HPO
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
0.100 Biomarker phenotype HPO
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay
0.100 Biomarker disease HPO
Serum chloride level decreased (finding)
0.100 Biomarker phenotype HPO
Hypokalemic hypochloremic metabolic alkalosis
0.100 Biomarker disease HPO
Decreased glomerular filtration rate
0.100 Biomarker phenotype HPO
CUI: C1846347
Disease: Renal salt wasting
Renal salt wasting
0.100 Biomarker phenotype HPO
CUI: C1846351
Disease: Increased urinary potassium
Increased urinary potassium
0.100 Biomarker phenotype HPO
CUI: C1846352
Disease: Hyperchloriduria
Hyperchloriduria
0.100 Biomarker phenotype HPO
CUI: C1854301
Disease: Motor delay
Motor delay
0.100 Biomarker phenotype HPO