Pages that link to "Template:WS"
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The following pages link to Template:WS:
Displaying 50 items.
- Dubowitz syndrome (← links)
- Episodic ataxia (← links)
- Familial dysautonomia (← links)
- Fibrous dysplasia (← links)
- Fragile X syndrome (← links)
- Frontotemporal dementia and parkinsonism linked to chromosome 17 (← links)
- Gardner's syndrome (← links)
- Greig cephalopolysyndactyly syndrome (← links)
- Hunter syndrome (← links)
- Huntington's disease (← links)
- Hypermethioninemia (← links)
- Infantile neuroaxonal dystrophy (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links)
- Joubert syndrome (← links)
- Leopard syndrome (← links)
- Liddle's syndrome (← links)
- Lipoid congenital adrenal hyperplasia (← links)
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (← links)
- Maple syrup urine disease (← links)
- Meckel syndrome (← links)
- Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (← links)
- Muscular dystrophy (← links)
- Myotonia congenita (← links)
- Neurofibromatosis type II (← links)
- Norrie disease (← links)
- Omenn syndrome (← links)
- Ornithine translocase deficiency (← links)
- Otospondylomegaepiphyseal dysplasia (← links)
- Pachyonychia congenita (← 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)
- Pseudoachondroplasia (transclusion) (← links)
- Recessive multiple epiphyseal dysplasia (transclusion) (← links)
- Refsum's syndrome (transclusion) (← links)
- Rett syndrome (transclusion) (← links)
- Ring chromosome 18 syndrome (transclusion) (← links)
- Rubinstein-Taybi syndrome (transclusion) (← links)
- Salla disease (transclusion) (← links)
- Sarcosinemia (transclusion) (← links)
- Short-chain acyl-coenzyme A dehydrogenase deficiency (transclusion) (← links)