SEPTIN9, septin 9, 10801

N. diseases: 150; N. variants: 26
Disease: Brachial Neuralgia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0085920
Disease: Brachial Neuralgia
Brachial Neuralgia 		0.300 Biomarker disease CTD_human SEPT9 sequence alternations causing hereditary neuralgic amyotrophy are associated with altered interactions with SEPT4/SEPT11 and resistance to Rho/Rhotekin-signaling. 17546647 2007