Match patient symptoms to candidate ciliary genes using HPO terms, canonical symptoms, organ systems, or disease names. Curated from 5,752 OMIM clinical-synopsis records across 52 ciliopathy disease entities (Supplementary Table S2 v6.1).
Type any combination of HPO IDs, symptom names, organ systems, or disease names. The matcher recognizes all four input types and returns ranked candidate ciliary genes by IC-weighted phenotype similarity.