Congenital craniostenosis with syndactyly.

Synonyms: Disease, Apert-Crouzon, Chotzen Syndrome, Saethre Chotzen Syndrome, Acrocephalosyndactyly IIIs, Syndactylic Oxycephaly, Acrocephalosyndactylia, Acrocephalosyndactylies, Type 3, Syndrome, Chotzen, Syndromes, Noack, Type I Acrocephalosyndactylies, Noack Syndrome, Acrocephalosyndactylies, Type 1, Type III Acrocephalosyndactyly, Acrocephalosyndactyly, Type I, Acrocephaly, Skull Asymmetry, and Mild Syndactyly, Saethre-Chotzen Syndrome, Acrocephalosyndactyly, Type V, Acrocephalosyndactylies, Type II, Kurczynski Casperson Syndrome, Syndrome, Apert, Syndrome, Noack, Apert Syndrome, Type V Acrocephalosyndactyly, Pfeiffer Syndrome, Acrocephalosyndactylies, Type I, Type V Acrocephalosyndactylies, Acrocephalosyndactyly, Type III, Acrocephalosyndactyly, Type II, Noack Syndromes, Acrocephalosyndactylias, Type II Acrocephalosyndactylies, Acrocephalosyndactyly III, Type II Acrocephalosyndactyly, Syndactylic Oxycephalies, Apert Crouzon Disease, Syndrome, Kurczynski Casperson, Syndrome, Pfeiffer, Acrocephalosyndactyly (Apert), Acrocephalosyndactylies, Type V, Type I Acrocephalosyndactyly, Apert-Crouzon Disease, Craniofacial-Skeletal-Dermatologic Dysplasia, Acrocephalosyndactylies, Type III, Dysostosis Craniofacialis with Hypertelorism, Acrocephalosyndactyly, Type 3, Syndrome, Saethre-Chotzen, Acrocephalosyndactyly, Type 1