rs587779411, CLN8

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Progressive psychomotor deterioration
CUI: C1856565
Disease: Progressive psychomotor deterioration
0.700 CausalMutation CLINVAR
Generalized cerebral atrophy/hypoplasia
CUI: C4024945
Disease: Generalized cerebral atrophy/hypoplasia
0.700 CausalMutation CLINVAR
CEROID LIPOFUSCINOSIS, NEURONAL, 8
CUI: C1838570
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 8
0.700 CausalMutation CLINVAR
Neuronal Ceroid-Lipofuscinoses
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
0.700 GeneticVariation CLINVAR
Complex partial seizure with impairment of consciousness
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
0.700 CausalMutation CLINVAR