PDCD10, programmed cell death 10, 11235

N. diseases: 68; N. variants: 11
Disease: Familial cerebral cavernous malformation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931263
Disease: Familial cerebral cavernous malformation
Familial cerebral cavernous malformation 		0.510 Biomarker disease MGD
CUI: C2931263
Disease: Familial cerebral cavernous malformation
Familial cerebral cavernous malformation 		0.510 Biomarker disease GENOMICS_ENGLAND Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations. 15543491 2005
CUI: C2931263
Disease: Familial cerebral cavernous malformation
Familial cerebral cavernous malformation 		0.510 GeneticVariation disease BEFREE Familial cerebral cavernous malformation (FCCM) is a vascular malformation disorder that closely associated with three identified genes: KRIT1/CCM1, MGC4607/CCM2, and PDCD10/CCM3. 28160210 2017