Source: CURATED ×
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Abnormal delivery
CUI: C0549629
Disease: Abnormal delivery
0.700 GeneticVariation CLINVAR
Left ventricular noncompaction
CUI: C1960469
Disease: Left ventricular noncompaction
0.700 GeneticVariation CLINVAR
Astigmatism
CUI: C0004106
Disease: Astigmatism
0.700 GeneticVariation CLINVAR
Malrotation of kidney
CUI: C0238210
Disease: Malrotation of kidney
0.700 GeneticVariation CLINVAR
Breech Presentation
CUI: C0006157
Disease: Breech Presentation
0.700 GeneticVariation CLINVAR
Flatfoot
CUI: C0016202
Disease: Flatfoot
0.700 GeneticVariation CLINVAR
Thin lips
CUI: C0578038
Disease: Thin lips
0.700 GeneticVariation CLINVAR
Status Epilepticus
CUI: C0038220
Disease: Status Epilepticus
0.700 GeneticVariation CLINVAR
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 GeneticVariation CLINVAR
Widely-spaced maxillary central incisors
0.700 GeneticVariation CLINVAR
Cupped ears (finding)
CUI: C1845447
Disease: Cupped ears (finding)
0.700 GeneticVariation CLINVAR
Arachnodactyly
CUI: C0003706
Disease: Arachnodactyly
0.700 GeneticVariation CLINVAR
Self-Injurious Behavior
CUI: C0085271
Disease: Self-Injurious Behavior
0.700 GeneticVariation CLINVAR
Amblyopia
CUI: C0002418
Disease: Amblyopia
0.700 GeneticVariation CLINVAR
Feeding difficulties
CUI: C0232466
Disease: Feeding difficulties
0.700 GeneticVariation CLINVAR
Reduced fetal movement
CUI: C0235659
Disease: Reduced fetal movement
0.700 GeneticVariation CLINVAR
Complex partial seizure with impairment of consciousness
0.700 GeneticVariation CLINVAR
Cerebellar atrophy
CUI: C0740279
Disease: Cerebellar atrophy
0.700 GeneticVariation CLINVAR
Aggressive behavior
CUI: C0001807
Disease: Aggressive behavior
0.700 GeneticVariation CLINVAR
Focal glomerulosclerosis
CUI: C0017668
Disease: Focal glomerulosclerosis
0.700 GeneticVariation CLINVAR
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
0.700 GeneticVariation CLINVAR
Narrow foot
CUI: C0576227
Disease: Narrow foot
0.700 GeneticVariation CLINVAR
Overfolded helix
CUI: C1837731
Disease: Overfolded helix
0.700 GeneticVariation CLINVAR
Prolonged QT interval
CUI: C0151878
Disease: Prolonged QT interval
0.700 GeneticVariation CLINVAR
Sleep Apnea, Obstructive
CUI: C0520679
Disease: Sleep Apnea, Obstructive
0.700 GeneticVariation CLINVAR