DNMT1, DNA methyltransferase 1, 1786

N. diseases: 496; N. variants: 36
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		0.300 Biomarker disease CTD_human Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss. 21532572 2011