Disease: PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1842687
Disease: PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder)
PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder) 		0.700 Biomarker disease GENOMICS_ENGLAND Loss of PCLO function underlies pontocerebellar hypoplasia type III. 25832664 2015
CUI: C1842687
Disease: PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder)
PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder) 		0.700 GermlineCausalMutation disease ORPHANET Loss of PCLO function underlies pontocerebellar hypoplasia type III. 25832664 2015
CUI: C1842687
Disease: PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder)
PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder) 		0.700 Biomarker disease GENOMICS_ENGLAND Loss of PCLO function underlies pontocerebellar hypoplasia type III. 25832664 2015
CUI: C1842687
Disease: PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder)
PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder) 		0.700 Biomarker disease CTD_human
CUI: C1842687
Disease: PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder)
PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder) 		0.700 CausalMutation disease CLINVAR