obsolete_Catel-Manzke syndrome true Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome OMIM:302380 Index finger anomaly - Pierre Robin syndrome Palatodigital syndrome, Catel-Manzke type Pierre Robin sequence - hyperphalangy - clinodactyly OMIM:616145 UMLS:C1844887 3.41.0 ICD10:Q87.8 Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence (see this term) comprising micrognathia, cleft palate and glossoptosis. Replaced with Mondo term. Pierre Robin syndrome - hyperphalangy - clinodactyly http://purl.obolibrary.org/obo/MONDO_0014507 Micrognathia digital syndrome MESH:C535347 orphanet