Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.500 GermlineCausalMutation ORPHANET Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis. 25261971

2014
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.500 GermlineCausalMutation ORPHANET Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis? 25348633

2014
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.500 GermlineCausalMutation ORPHANET Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease. 25113787

2014
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.500 GermlineCausalMutation ORPHANET Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease. 25113788

2014
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.500 GermlineCausalMutation ORPHANET Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis? 25348631

2014
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.500 GermlineCausalMutation ORPHANET Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis. 25261972

2014
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.500 GermlineCausalMutation ORPHANET This study demonstrates the implication of CHCHD10 in FTD and ALS spectrum. 25155093

2014