DCC, DCC netrin 1 receptor, 1630

N. diseases: 279; N. variants: 101
Disease: Gaze Palsy, Familial Horizontal, with Progressive Scoliosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1846496
Disease: Gaze Palsy, Familial Horizontal, with Progressive Scoliosis
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 		0.300 GermlineCausalMutation disease ORPHANET Biallelic mutations in human DCC cause developmental split-brain syndrome. 28250456 2017