DNAL4, dynein axonemal light chain 4, 10126

N. diseases: 15; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4015124
Disease: MIRROR MOVEMENTS 3
MIRROR MOVEMENTS 3 		0.400 CausalMutation disease CLINVAR
CUI: C4015124
Disease: MIRROR MOVEMENTS 3
MIRROR MOVEMENTS 3 		0.400 Biomarker disease CTD_human
CUI: C0454455
Disease: Mirror movements disorder
Mirror movements disorder 		0.110 GeneticVariation disease BEFREE Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder. 25098561 2014
CUI: C0454455
Disease: Mirror movements disorder
Mirror movements disorder 		0.110 Biomarker disease HPO
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.100 GeneticVariation phenotype GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		0.100 Biomarker disease HPO
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		0.100 Biomarker disease HPO
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum 		0.100 Biomarker disease HPO
CUI: C0231528
Disease: Myalgia
Myalgia 		0.100 Biomarker phenotype HPO
CUI: C0233844
Disease: Clumsiness
Clumsiness 		0.100 Biomarker phenotype HPO
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.100 Biomarker disease HPO
CUI: C1837098
Disease: Easy fatigability
Easy fatigability 		0.100 Biomarker phenotype HPO
CUI: C1867864
Disease: Poor fine motor coordination
Poor fine motor coordination 		0.100 Biomarker phenotype HPO
CUI: C3887527
Disease: Fused cervical vertebrae
Fused cervical vertebrae 		0.100 Biomarker disease HPO
CUI: C4025704
Disease: Abnormality of the corticospinal tract
Abnormality of the corticospinal tract 		0.100 Biomarker phenotype HPO
CUI: C4025790
Disease: Specific learning disability
Specific learning disability 		0.100 Biomarker disease HPO
CUI: C4476591
Disease: Dysgenesis of the hippocampus
Dysgenesis of the hippocampus 		0.100 Biomarker disease HPO