The association between C9orf72 (C9orf72-SMCR8 Complex Subunit) and Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.
Sources3
Clinical variants0
Symptoms107
Compounds0
Trials0
Publications1
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.