Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Charcot-Marie-Tooth disease, X-linked, 1
0.040 GeneticVariation disease BEFREE X-linked Charcot-Marie-Tooth neuropathy (CMTX), which has clinical features similar to CMT1, is associated with mutations in the connexin32 gene. 11345007 2001
Charcot-Marie-Tooth disease, X-linked, 1
0.040 GeneticVariation disease BEFREE X-linked Charcot-Marie-Tooth neuropathy (CMTX), which has clinical features similar to CMT1, is associated with mutations in the connexin32 gene. 10219749 1999
Charcot-Marie-Tooth disease, X-linked, 1
0.040 GeneticVariation disease BEFREE X-linked Charcot-Marie-Tooth neuropathy (CMTX), which has clinical features similar to CMT1, is associated with mutations in the connexin32 gene. 10716658 1999
Charcot-Marie-Tooth disease, X-linked, 1
0.040 GeneticVariation disease BEFREE Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a genetically heterogeneous group of chronic demyelinating polyneuropathies with loci mapping to chromosome 17 (CMT1A), chromosome 1 (CMT1B), the X chromosome (CMTX) and to another unknown autosome (CMT1C). 7849745 1994