Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy
0.110 GeneticVariation disease BEFREE Mutations in GDAP1 lead to severe forms of the peripheral motor and sensory neuropathy, Charcot-Marie-Tooth disease (CMT), which is characterized by heterogeneous phenotypes, including pronounced axonal damage and demyelination. 16172208 2005
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy
0.110 CausalMutation disease CLINVAR