Pages that link to "Template:WS"
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The following pages link to Template:WS:
Displaying 50 items.
- Glutathione synthetase deficiency (transclusion) (← links)
- Greig cephalopolysyndactyly syndrome (transclusion) (← links)
- Guanidinoacetate methyltransferase deficiency (transclusion) (← links)
- Health aspects of Down syndrome (transclusion) (← links)
- Hunter syndrome (transclusion) (← links)
- Huntington's disease (transclusion) (← links)
- Hyperlysinemia (transclusion) (← links)
- Hypermethioninemia (transclusion) (← links)
- Hyperprolinemia (transclusion) (← links)
- Hypochondrogenesis (transclusion) (← links)
- Infantile neuroaxonal dystrophy (transclusion) (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (transclusion) (← links)
- Joubert syndrome (transclusion) (← links)
- Leopard syndrome (transclusion) (← links)
- Liddle's syndrome (transclusion) (← links)
- Lipoid congenital adrenal hyperplasia (transclusion) (← links)
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (transclusion) (← links)
- Lysinuric protein intolerance (transclusion) (← links)
- Léri-Weill dyschondrosteosis (transclusion) (← links)
- Malonyl-CoA decarboxylase deficiency (transclusion) (← links)
- Maple syrup urine disease (transclusion) (← links)
- Meckel syndrome (transclusion) (← links)
- Microphthalmia (transclusion) (← links)
- Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (transclusion) (← links)
- Muscular dystrophy (transclusion) (← links)
- Myelokathexis (transclusion) (← links)
- Myeloperoxidase deficiency (transclusion) (← links)
- Myotonia congenita (transclusion) (← links)
- Nephronophthisis (transclusion) (← links)
- Neurofibromatosis type II (transclusion) (← links)
- Norrie disease (transclusion) (← links)
- Nullisomic (transclusion) (← links)
- Omenn syndrome (transclusion) (← links)
- Ornithine translocase deficiency (transclusion) (← links)
- Otospondylomegaepiphyseal dysplasia (transclusion) (← links)
- Polychromia (transclusion) (← links)
- Pachyonychia congenita (transclusion) (← links)
- Paroxysmal extreme pain disorder (transclusion) (← links)
- Pendred syndrome (transclusion) (← links)
- Pentose phosphate pathway (transclusion) (← links)
- Periodic paralysis (transclusion) (← links)
- Peutz-Jeghers syndrome (transclusion) (← links)
- Photic sneeze reflex (transclusion) (← links)
- Platyspondylic lethal skeletal dysplasia, Torrance type (transclusion) (← links)
- Polycystic kidney disease (transclusion) (← links)
- Polysomy (transclusion) (← links)
- Porphyria cutanea tarda (transclusion) (← links)
- Potassium-aggravated myotonia (transclusion) (← links)
- Prolidase deficiency (transclusion) (← links)
- Propionic acidemia (transclusion) (← links)