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 		0.300 Biomarker disease GENOMICS_ENGLAND Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type I. 20920666 2010