Disease: Benign paroxysmal torticollis of infancy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3494934
Disease: Benign paroxysmal torticollis of infancy
Benign paroxysmal torticollis of infancy 		0.300 GermlineCausalMutation phenotype ORPHANET Benign paroxysmal torticollis of infancy: four new cases and linkage to CACNA1A mutation. 12162387 2002