Misplaced Pages

The following pages link to X-linked adrenal hypoplasia congenita

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• Feingold syndrome (links | edit)
• DAX1 (links | edit)
• Brunner syndrome (links | edit)
• Ohtahara syndrome (links | edit)
• Adrenal hypoplasia (redirect page) (links | edit)
  • List of diseases (A) (links | edit)
  • Microtia (links | edit)
  • 3C syndrome (links | edit)
  • Genetics of GnRH deficiency conditions (links | edit)
  • Pituitary stalk interruption syndrome (links | edit)
  • Talk:Kallmann syndrome (links | edit)
  • Talk:Adrenal hypoplasia (links | edit)
  • User:Wenli (links | edit)
  • User:Neilsmith38/sandbox (links | edit)
  • User:Karishma.Patel.8/Pituitary Stalk Interruption Syndrome (links | edit)
  • User talk:Anandks007/Med (links | edit)
  • Misplaced Pages:Version 1.0 Editorial Team/Medicine articles by quality log (links | edit)
  • Misplaced Pages:Version 1.0 Editorial Team/Medical genetics articles by quality log (links | edit)
  • Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
• SAMD9 (links | edit)
• Adrenal hypoplasia congenital, X-linked (redirect page) (links | edit)
  • List of diseases (A) (links | edit)
  • Talk:Adrenal hypoplasia congenital, X-linked (links | edit)
  • User talk:Anandks007/Med (links | edit)
  • Misplaced Pages:Version 1.0 Editorial Team/Medicine articles by quality log (links | edit)
  • Misplaced Pages:Version 1.0 Editorial Team/Medical genetics articles by quality log (links | edit)
  • Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
• X-linked lymphoproliferative disease (links | edit)
• Acrocallosal syndrome (links | edit)
• Ocular albinism (links | edit)
• Orofaciodigital syndrome 1 (links | edit)
• Contiguous gene syndrome (links | edit)
• Iridogoniodysgenesis, dominant type (links | edit)
• Focal dermal hypoplasia (links | edit)
• CHILD syndrome (links | edit)
• Ocular albinism type 1 (links | edit)
• X-linked intellectual disability (links | edit)
• Danon disease (links | edit)
• FG syndrome (links | edit)
• Atrichia with papular lesions (links | edit)
• Rapp–Hodgkin syndrome (links | edit)
• Tooth and nail syndrome (links | edit)
• Synpolydactyly (links | edit)
• Familial partial lipodystrophy (links | edit)
• Autoimmune polyendocrine syndrome type 1 (links | edit)
• Gillespie syndrome (links | edit)
• MODY 1 (links | edit)
• MODY 3 (links | edit)
• MODY 4 (links | edit)
• Renal cysts and diabetes syndrome (links | edit)
• Transient neonatal diabetes (links | edit)
• X-linked spinal muscular atrophy type 2 (links | edit)
• Enlarged vestibular aqueduct (links | edit)
• MODY 6 (links | edit)
• Lujan–Fryns syndrome (links | edit)
• X-linked myotubular myopathy (links | edit)
• Yemenite deaf-blind hypopigmentation syndrome (links | edit)
• Ulnar–mammary syndrome (links | edit)
• Anterior segment mesenchymal dysgenesis (links | edit)
• Complete androgen insensitivity syndrome (links | edit)
• Alveolar capillary dysplasia (links | edit)
• Smith–Fineman–Myers syndrome (links | edit)
• Pitt–Hopkins syndrome (links | edit)
• Mohr–Tranebjærg syndrome (links | edit)
• Bamforth–Lazarus syndrome (links | edit)
• Limb–mammary syndrome (links | edit)
• Mild androgen insensitivity syndrome (links | edit)
• Hypotrichosis–lymphedema–telangiectasia syndrome (links | edit)
• Amelogenesis imperfecta (links | edit)
• Nasodigitoacoustic syndrome (links | edit)