rs1247665387, FA2H

N. diseases: 14
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Syncope
CUI: C0039070
Disease: Syncope
0.700 GeneticVariation CLINVAR
Delayed speech and language development
CUI: C0454644
Disease: Delayed speech and language development
0.700 GeneticVariation CLINVAR
Gait abnormality
CUI: C0575081
Disease: Gait abnormality
0.700 GeneticVariation CLINVAR
Developmental regression
CUI: C1836830
Disease: Developmental regression
0.700 GeneticVariation CLINVAR
Secondary Caesarian section
CUI: C4072904
Disease: Secondary Caesarian section
0.700 GeneticVariation CLINVAR
Neurogenic Urinary Bladder
CUI: C0005697
Disease: Neurogenic Urinary Bladder
0.700 GeneticVariation CLINVAR
Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia
CUI: C3496228
Disease: Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia
0.700 GeneticVariation CLINVAR
Dystonia
CUI: C0013421
Disease: Dystonia
0.700 GeneticVariation CLINVAR
Motor delay
CUI: C1854301
Disease: Motor delay
0.700 GeneticVariation CLINVAR
Maternal hypertension
CUI: C0565599
Disease: Maternal hypertension
0.700 GeneticVariation CLINVAR
Flexion contracture
CUI: C0333068
Disease: Flexion contracture
0.700 GeneticVariation CLINVAR
Abnormal delivery
CUI: C0549629
Disease: Abnormal delivery
0.700 GeneticVariation CLINVAR
Muscle Spasticity
CUI: C0026838
Disease: Muscle Spasticity
0.700 GeneticVariation CLINVAR
Hip Dysplasia
CUI: C1328407
Disease: Hip Dysplasia
0.700 GeneticVariation CLINVAR