Abell 2142Adam & YvesAllan–Herndon–Dudley syndromeBarth syndromeBecker's muscular dystrophyCreatine transporter defectDahlberg Borer Newcomer syndromeDent's diseaseDuchenne muscular dystrophyGlucose-6-phosphate dehydrogenase deficiencyGlycerol kinase deficiencyHyper-IgM syndrome type 1Keratosis follicularis spinulosa decalvansKeyboard MaestroLujan–Fryns syndromeMASA syndromeMECP2 duplication syndromeMcLeod syndromeMenkes diseaseMohr–Tranebjærg syndromeOccipital horn syndromeOculocerebrorenal syndromeOnce Upon a GirlOrofaciodigital syndrome 1Properdin deficiencyRehal (book rest)Say–Meyer syndromeSmith–Fineman–Myers syndromeThe Life and Times of Xaviera HollanderWiskott–Aldrich syndromeX-linked agammaglobulinemiaX-linked congenital stationary night blindnessX-linked hypophosphatemia