Disease: Central hypotonia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1842364
Disease: Central hypotonia
Central hypotonia 		0.300 Biomarker phenotype GENOMICS_ENGLAND Clinical characterization, genetic mapping and whole-genome sequence analysis of a novel autosomal recessive intellectual disability syndrome. 25078763 2014