Misplaced Pages

The following pages link to Hunter syndrome

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• Spinal and bulbar muscular atrophy (links | edit)
• Β-Glucuronidase (links | edit)
• X-linked agammaglobulinemia (links | edit)
• Morquio syndrome (links | edit)
• Sideroblastic anemia (links | edit)
• Mucopolysaccharidosis, type II (redirect page) (links | edit)
• Hunter's syndrome (redirect page) (links | edit)
• Dyskeratosis congenita (links | edit)
• Enzyme replacement therapy (links | edit)
• X-linked adrenal hypoplasia congenita (links | edit)
• Hunter Syndrome (redirect page) (links | edit)
  • User:The Anome/Compassionate allowance conditions (links | edit)
  • User:Mroseb21/sandbox (links | edit)
  • User:Michelangelo1992 (links | edit)
• Nephrogenic diabetes insipidus (links | edit)
• List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
• Choroideremia (links | edit)
• IPEX syndrome (links | edit)
• Simpson–Golabi–Behmel syndrome (links | edit)
• Wulver (links | edit)
• X-linked severe combined immunodeficiency (links | edit)
• Lewes Crown Court (links | edit)
• Centronuclear myopathy (links | edit)
• Transcytosis (links | edit)
• Mucopolysaccharidosis ii (redirect page) (links | edit)
  • List of MeSH codes (C17) (links | edit)
  • List of MeSH codes (C10) (links | edit)
  • User:Brainist/MeSH articles (links | edit)
• Oculocerebrorenal syndrome (links | edit)
• ATR-X syndrome (links | edit)
• Emery–Dreifuss muscular dystrophy (links | edit)
• McLeod syndrome (links | edit)
• Partial androgen insensitivity syndrome (links | edit)
• Iduronidase (links | edit)
• X-linked dominant inheritance (links | edit)
• X-linked hypophosphatemia (links | edit)
• Hypohidrotic ectodermal dysplasia (links | edit)
• Arylsulfatase B (links | edit)
• Maroteaux–Lamy syndrome (links | edit)
• Conradi–Hünermann syndrome (links | edit)
• Iduronate-2-sulfatase (links | edit)
• Samuel Conway (links | edit)
• Hyper-IgM syndrome type 1 (links | edit)
• Craniofrontonasal dysplasia (links | edit)
• Properdin deficiency (links | edit)
• Dent's disease (links | edit)
• Galactosamine-6 sulfatase (links | edit)
• Α-N-Acetylglucosaminidase (links | edit)
• N-acetylglucosamine-6-sulfatase (links | edit)
• Scheie syndrome (links | edit)
• Idursulfase (links | edit)
• Hurler–Scheie syndrome (links | edit)
• Brunner syndrome (links | edit)
• GLB1 (links | edit)
• EXT1 (links | edit)
• EXT2 (gene) (links | edit)