TENM4, teneurin transmembrane protein 4, 26011

N. diseases: 44; N. variants: 52
Disease: TREMOR, HEREDITARY ESSENTIAL, 5 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.600 GeneticVariation disease UNIPROT Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor. 26188006 2015
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.600 Biomarker disease CTD_human
CUI: C4225223
Disease: TREMOR, HEREDITARY ESSENTIAL, 5
TREMOR, HEREDITARY ESSENTIAL, 5 		0.600 CausalMutation disease CLINVAR