rs1565869918, FGD4

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
CUI: C1836336
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
0.700 CausalMutation CLINVAR
Abnormal peripheral nervous system morphology
CUI: C4025831
Disease: Abnormal peripheral nervous system morphology
0.700 CausalMutation CLINVAR
Peripheral demyelinating neuropathy
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
0.700 CausalMutation CLINVAR