Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		0.110 GeneticVariation 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
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		0.110 CausalMutation CLINVAR