Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly
0.100 Biomarker disease HPO
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly
0.100 CausalMutation disease CLINVAR
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack
0.100 Biomarker disease HPO
CUI: C0008031
Disease: Chest Pain
Chest Pain
0.100 Biomarker phenotype HPO
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
0.100 Biomarker disease HPO
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
0.100 Biomarker disease HPO
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.100 Biomarker disease HPO
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
0.100 Biomarker disease HPO
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus
0.100 Biomarker disease HPO
CUI: C0013405
Disease: Dyspnea, Paroxysmal
Dyspnea, Paroxysmal
0.100 Biomarker disease HPO
CUI: C0015300
Disease: Exophthalmos
Exophthalmos
0.100 Biomarker disease HPO
CUI: C0015310
Disease: Exotropia
Exotropia
0.100 Biomarker disease HPO
CUI: C0016202
Disease: Flatfoot
Flatfoot
0.100 Biomarker phenotype HPO
CUI: C0016202
Disease: Flatfoot
Flatfoot
0.100 CausalMutation phenotype CLINVAR
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
0.100 Biomarker disease HPO
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest
0.100 Biomarker disease HPO
CUI: C0018800
Disease: Cardiomegaly
Cardiomegaly
0.100 Biomarker phenotype HPO
CUI: C0019079
Disease: Hemoptysis
Hemoptysis
0.100 Biomarker phenotype HPO
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal
0.100 Biomarker phenotype HPO
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
0.100 Biomarker phenotype HPO
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.100 Biomarker disease HPO
CUI: C0027092
Disease: Myopia
Myopia
0.100 CausalMutation disease CLINVAR
CUI: C0032326
Disease: Pneumothorax
Pneumothorax
0.100 Biomarker phenotype HPO
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.100 Biomarker disease HPO
CUI: C0037268
Disease: Skin Abnormalities
Skin Abnormalities
0.100 Biomarker group HPO