BDNF-AS, BDNF antisense RNA, 497258

N. diseases: 77; N. variants: 60
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0.100 GeneticVariation phenotype CLINVAR Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families. 28397838 2018
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0.100 GeneticVariation phenotype CLINVAR Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity. 23044507 2012
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0.100 GeneticVariation phenotype CLINVAR 11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity. 21567907 2011
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0.100 GeneticVariation phenotype CLINVAR New insights into the role of brain-derived neurotrophic factor in synaptic plasticity. 19577647 2009
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0.100 GeneticVariation phenotype CLINVAR Brain-derived neurotrophic factor and obesity in the WAGR syndrome. 18753648 2008
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0.100 GeneticVariation phenotype CLINVAR Conditional deletion of brain-derived neurotrophic factor in the postnatal brain leads to obesity and hyperactivity. 11579207 2001