Disease: Muscle Spasticity ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		0.130 GeneticVariation phenotype BEFREE Behavioral studies demonstrated slowed movement without muscle weakness in ALS2(-/-) mice, consistent with upper motor neuron defects that lead to spasticity in humans. 16802286 2006
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		0.130 GeneticVariation phenotype LHGDN Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families. 12601111 2003
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		0.130 GeneticVariation phenotype LHGDN Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene. 12145748 2002
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		0.130 Biomarker phenotype HPO