multiple congenital anomalies/dysmorphic syndrome without intellectual disability Charlie M syndrome https://rarediseases.info.nih.gov/diseases/1261/charlie-m-syndrome https://www.malacards.org/card/charlie_m_syndrome UMLS:C4518555 Orphanet:1406 MONDO:0015367 Charlie M syndrome is a rare bone developmental disorder which belongs to a group of oromandibular limb hypogenesis syndromes that includes hypoglossia-hypodactyly and glossopalatine ankylosis. The major anomalies which occur commonly in this group are hypoplasia of the mandible, syndactyly and ectrodactyly, small mouth, cleft palate, hypodontia, and facial paralysis. Patients with Charlie M syndrome also present with hypertelorism, absent or conically crowned incisors, and variable degrees of hypodactyly of the hands and feet. There have been no further descriptions in the literature since 1976. SCTID:733034007 GARD:0001261 icd11.foundation:1284734481 MEDGEN:1379887 oromandibular-limb hypogenesis syndrome