Misplaced Pages

The following pages link to Apert syndrome

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Showing 50 items.

• Superior rectus muscle (links | edit)
• Syndactyly (links | edit)
• Saethre–Chotzen syndrome (links | edit)
• CHARGE syndrome (links | edit)
• Fraser syndrome (links | edit)
• VACTERL association (links | edit)
• Leber congenital amaurosis (links | edit)
• Hypogammaglobulinemia (links | edit)
• Carpenter syndrome (links | edit)
• Hypochondroplasia (links | edit)
• Common variable immunodeficiency (links | edit)
• ABCD syndrome (links | edit)
• Hypertelorism (links | edit)
• Goldenhar syndrome (links | edit)
• Well-Schooled in Murder (links | edit)
• Chromosome 10 (links | edit)
• Jackson–Weiss syndrome (links | edit)
• Pfeiffer syndrome (links | edit)
• Nephrogenic diabetes insipidus (links | edit)
• Pseudohypoparathyroidism (links | edit)
• Familial male-limited precocious puberty (links | edit)
• Fountain syndrome (links | edit)
• List of ICD-9 codes 740–759: congenital anomalies (links | edit)
• Caudal regression syndrome (links | edit)
• Bannayan–Riley–Ruvalcaba syndrome (links | edit)
• Apert's syndrome (redirect page) (links | edit)
  • Acne (links | edit)
  • Metacarpal synostosis (links | edit)
• X-linked severe combined immunodeficiency (links | edit)
• Seckel syndrome (links | edit)
• Selective immunoglobulin A deficiency (links | edit)
• Nevoid basal-cell carcinoma syndrome (links | edit)
• Piebaldism (links | edit)
• Laurence–Moon syndrome (links | edit)
• Robinow syndrome (links | edit)
• Primordial dwarfism (links | edit)
• Holt–Oram syndrome (links | edit)
• Nail–patella syndrome (links | edit)
• XX gonadal dysgenesis (links | edit)
• Acrocephalosyndactyly (Apert) (redirect page) (links | edit)
• Catel–Manzke syndrome (links | edit)
• Pierre Robin sequence (links | edit)
• Acrocephalosyndactyly (links | edit)
• Hearing loss with craniofacial syndromes (links | edit)
• TNF receptor associated periodic syndrome (links | edit)
• Loeys–Dietz syndrome (links | edit)
• Webbed toes (links | edit)
• Hypohidrotic ectodermal dysplasia (links | edit)
• Ectromelia (links | edit)
• Familial hypercholesterolemia (links | edit)
• Hemimegalencephaly (links | edit)
• Twist-related protein 1 (links | edit)