CLTCL1, clathrin heavy chain like 1, 8218

N. diseases: 9; N. variants: 62
Disease: Congenital Pain Insensitivity ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		0.300 Biomarker disease GENOMICS_ENGLAND A novel disorder reveals clathrin heavy chain-22 is essential for human pain and touch development. 26068709 2015
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		0.300 Biomarker disease GENOMICS_ENGLAND A novel disorder reveals clathrin heavy chain-22 is essential for human pain and touch development. 26068709 2015