Disease: Neurodevelopmental Disorders ×
Source: BEFREE ×
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neurodevelopmental Disorders
CUI: C1535926
Disease: Neurodevelopmental Disorders
0.010 GeneticVariation BEFREE An X-linked neurodevelopmental disorder previously had been reported in only one family, associated with a p.D59G mutation in the RAB40AL gene that encodes a mitochondrial Ras protein. 24863632 2014