Disease: Dysautonomia, Familial ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013364
Disease: Dysautonomia, Familial
Dysautonomia, Familial 		0.010 GeneticVariation disease BEFREE TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability. 26542466 2016