Phenotypic similarity network between individuals with AHDC1 variants and OMIM diseases
(A) Clustering of individuals with an AHDC1 missense mutation or truncation mutation with 3,464 diseases reported to OMIM based on phenotype similarity illustrated by orange dots, blue dots, and green dots, respectively.
(B) Reclustered OMIM disease nodes with at least one connection and similarity >0.1 to individuals with an AHDC1 missense or truncation mutation.