has material basis in germline mutation in TGDS syndromic intellectual disability Catel-Manzke syndrome https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/6751 https://github.com/monarch-initiative/mondo/issues/6877 https://rarediseases.info.nih.gov/diseases/28/catel-manzke-syndrome https://www.malacards.org/card/catel_manzke_syndrome_2 NORD:901 OMIM:302380 Catel-Manzke syndrome DOID:0081122 Catel Manzke syndrome Pierre Robin syndrome-hyperphalangy-clinodactyly syndrome OMIM:616145 UMLS:C1844887 Orphanet:1388 hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome CATMANS 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 comprising micrognathia, cleft palate and glossoptosis. GARD:0000028 MEDGEN:375536 Catel Manzke Syndrome SCTID:722383001 Palatodigital syndrome Catel-Manzke type index finger anomaly-Pierre Robin syndrome MONDO:0014507 icd11.foundation:1023183031 Palatodigital syndrome, Catel-Manzke type micrognathia digital syndrome Pierre Robin sequence-hyperphalangy-clinodactyly syndrome MESH:C535347 multiple congenital anomalies/dysmorphic syndrome-intellectual disability skeletal dysplasia