Disease: Hereditary Sensory Autonomic Neuropathy, Type 5 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		0.520 GeneticVariation disease BEFREE No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V. 12210794 2002
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		0.520 GeneticVariation disease BEFREE A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V. 11310631 2001
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		0.520 GeneticVariation disease ORPHANET A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V. 11310631 2001
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		0.520 Biomarker disease CTD_human