rs587776625, ADGRG1

N. diseases: 12
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cerebral dysmyelination
CUI: C1854885
Disease: Cerebral dysmyelination
0.700 CausalMutation CLINVAR
POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
CUI: C1847352
Disease: POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
0.700 CausalMutation CLINVAR
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
0.700 CausalMutation CLINVAR
Impaired toileting ability
CUI: C4476941
Disease: Impaired toileting ability
0.700 CausalMutation CLINVAR
Poor school performance
CUI: C1843367
Disease: Poor school performance
0.700 CausalMutation CLINVAR
Cortical Dysplasia
CUI: C0431380
Disease: Cortical Dysplasia
0.700 CausalMutation CLINVAR
Delayed speech and language development
CUI: C0454644
Disease: Delayed speech and language development
0.700 CausalMutation CLINVAR
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 CausalMutation CLINVAR
Polymicrogyria
CUI: C0266464
Disease: Polymicrogyria
0.700 CausalMutation CLINVAR
Infantile muscular hypotonia
CUI: C1860834
Disease: Infantile muscular hypotonia
0.700 CausalMutation CLINVAR
Seizures
CUI: C0036572
Disease: Seizures
0.700 CausalMutation CLINVAR
Gait imbalance
CUI: C1836150
Disease: Gait imbalance
0.700 CausalMutation CLINVAR