Showing 50 items.
- Color blindness (links | edit)
- Genetic disorder (links | edit)
- Haemophilia (links | edit)
- Muscular dystrophy (links | edit)
- Diabetes insipidus (links | edit)
- Androgen insensitivity syndrome (links | edit)
- Adrenoleukodystrophy (links | edit)
- Fragile X syndrome (links | edit)
- Pelizaeus–Merzbacher disease (links | edit)
- Rett syndrome (links | edit)
- Drosophila melanogaster (links | edit)
- Sex differences in medicine (links | edit)
- Haemophilia A (links | edit)
- Haemophilia B (links | edit)
- X chromosome (links | edit)
- Barth syndrome (links | edit)
- Colpocephaly (links | edit)
- XLR (links | edit)
- Von Willebrand disease (links | edit)
- Retinitis pigmentosa (links | edit)
- Glucose-6-phosphate dehydrogenase deficiency (links | edit)
- Occipital horn syndrome (links | edit)
- Ulster Scots people (links | edit)
- Methylmalonic acidemias (links | edit)
- Growth hormone deficiency (links | edit)
- Chronic granulomatous disease (links | edit)
- Pedigree chart (links | edit)
- Alport syndrome (links | edit)
- Refractive error (links | edit)
- MASA syndrome (links | edit)
- Aicardi syndrome (links | edit)
- Osteogenesis imperfecta (links | edit)
- Duchenne muscular dystrophy (links | edit)
- Becker muscular dystrophy (links | edit)
- Ornithine transcarbamylase deficiency (links | edit)
- Kallmann syndrome (links | edit)
- Lesch–Nyhan syndrome (links | edit)
- Hurler syndrome (links | edit)
- Menkes disease (links | edit)
- Thiazide (links | edit)
- Wiskott–Aldrich syndrome (links | edit)
- Incontinentia pigmenti (links | edit)
- Sex linkage (links | edit)
- Family history (medicine) (links | edit)
- Microphthalmia (links | edit)
- Coffin–Lowry syndrome (links | edit)
- X-linked ichthyosis (links | edit)
- Norrie disease (links | edit)
- Spinal and bulbar muscular atrophy (links | edit)
- X-linked agammaglobulinemia (links | edit)