Disease: Hemiplegia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018991
Disease: Hemiplegia
Hemiplegia 		0.140 Biomarker phenotype BEFREE This case report indicates that the diagnosis of FHM should be taken into account when a patient manifests migraine accompanied with hemiplegia, acute encephalopathy, and abnormal CSF. 31824404 2019
CUI: C0018991
Disease: Hemiplegia
Hemiplegia 		0.140 GeneticVariation phenotype BEFREE Patients with CACNA1A variants often show acute attacks with ataxia or hemiplegia till coma, sometimes related to unilateral brain oedema. 27651281 2017
CUI: C0018991
Disease: Hemiplegia
Hemiplegia 		0.140 GeneticVariation phenotype BEFREE We describe four individuals, spanning three generations of a family, with episodic ataxia without hemiplegia and confusion, in association with a CACNA1A mutation. 19624685 2010
CUI: C0018991
Disease: Hemiplegia
Hemiplegia 		0.140 GeneticVariation phenotype BEFREE A nonsense mutation in CACNA1A causes episodic ataxia and complaint of weakness, and may be associated with hemiplegia. 10408533 1999
CUI: C0018991
Disease: Hemiplegia
Hemiplegia 		0.140 Biomarker phenotype HPO