Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026848
Disease: Myopathy
Myopathy
0.110 GeneticVariation group BEFREE In contrast, milder forms of HADHB mutations cause the later onset of progressive axonal peripheral neuropathy (approximately 50-80%) and myopathy with or without episodic myoglobinuria. 30953623 2019
CUI: C0026848
Disease: Myopathy
Myopathy
0.110 Biomarker group HPO