Going ahead in the list of ARM gene super-family, we find that ARMC9 (OMIM: 617612; 2q37.1), encoding basal body protein, is involved in causing various disease phenotypes, including a syndromic form of intellectual disability [35], Vogt–Koyanagi–Harada disease [36], and Joubert syndrome-30 (JBTS30) in humans and ciliopathy phenotypes in zebrafish mutants [37]. This evidence concerns the gene ARMC9 and Intellectual disability.