SEPTIN9, septin 9, 10801

N. diseases: 150; N. variants: 26
Disease: Brachial Plexus Neuritis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0221759
Disease: Brachial Plexus Neuritis
Brachial Plexus Neuritis 		0.510 GeneticVariation disease BEFREE Hereditary NA is mainly linked to a mutation in the gene of the Septin-9 protein. 27263426 2017
CUI: C0221759
Disease: Brachial Plexus Neuritis
Brachial Plexus Neuritis 		0.510 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
CUI: C0221759
Disease: Brachial Plexus Neuritis
Brachial Plexus Neuritis 		0.510 SusceptibilityMutation disease ORPHANET