Congenital midface hypoplasia

Common: Achondroplasia; Chondrodysplasia punctata; Cleidocranial dysostosis; Crouzon syndrome; Treacher Collins syndrome; Trisomy 21
Uncommon: 3-M syndrome; Aarskog syndrome; Acrodysostosis; Acrofacial dysostosis Miller type; Acrofacial dysostosis Nager type; Acromesomelic dysplasia; Antley-Bixler syndrome; Apert syndrome; Atelosteogenesis; Binder syndrome; Bloom syndrome; Campomelic dysplasia; Chromosome 18:del(18q) syndrome; Cowden syndrome; Craniofrontonasal dysplasia; Distal arthrogryposis type 2A; Dysosteosclerosis; Dysostosis Stanescu type; Dyssegmental dysplasia; Fetal alcohol syndrome; Fetal valproate syndrome; Frontonasal dysplasia; GAPO syndrome; Gerodermia osteodysplastica; Hajdu-Cheney syndrome; Hallermann-Streiff syndrome; Hypochondroplasia; Keutel syndrome; Kyphomelic dysplasia; Larsen syndrome; Mandibuloacral dysplasia; Oculo-auriculo-vertebral spectrum; Osteoglophonic dysplasia; Otopalatodigital syndrome type 2; Progeria; Pyknodysostosis; Rieger syndrome; Schinzel-Giedion syndrome; Schneckenbecken dysplasia; Seckel syndrome; Silver-Russell syndrome; SPONASTRIME dysplasia; Stickler syndrome; Thanatophoric dysplasia; Trichorhinophalangeal dysplasia type 1; Trisomy 18; Weill-Marchesani syndrome; Weissenbacher-Zweymüller phenotype; Wildervanck syndrome; Yunis-Varon syndrome

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