MAD2L1BP, MAD2L1 binding protein, 9587

N. diseases: 61; N. variants: 6
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1847823
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F 		0.010 GeneticVariation disease BEFREE The CMT2 neuropathy in this family represents a novel genetic entity designated CMT2F. 11528513 2001