Pages that link to "Template:WS"
Jump to navigation
Jump to search
The following pages link to Template:WS:
Displaying 50 items.
- Craniofrontonasal syndrome (transclusion) (← links)
- Crouzon syndrome (transclusion) (← links)
- Crouzonodermoskeletal syndrome (transclusion) (← links)
- Diastrophic dysplasia (transclusion) (← links)
- Dihydropyrimidine dehydrogenase deficiency (transclusion) (← links)
- Dirty phenotypes (transclusion) (← links)
- Disaccharidase (transclusion) (← links)
- Distal Trisomy 10q (transclusion) (← links)
- Dk phocomelia syndrome (transclusion) (← links)
- Duane-radial ray syndrome (transclusion) (← links)
- Dubowitz syndrome (transclusion) (← links)
- Episodic ataxia (transclusion) (← links)
- Estrogen insensitivity syndrome (transclusion) (← links)
- Ethylmalonic encephalopathy (transclusion) (← links)
- Exinct (transclusion) (← links)
- Familial dysautonomia (transclusion) (← links)
- Fibrous dysplasia (transclusion) (← links)
- Fragile X syndrome (transclusion) (← links)
- Fraser syndrome (transclusion) (← links)
- Frontotemporal dementia and parkinsonism linked to chromosome 17 (transclusion) (← links)
- Fructose malabsorption (transclusion) (← links)
- Gardner's syndrome (transclusion) (← links)
- 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)