Pages that link to "Template:NLM"
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The following pages link to Template:NLM:
Displaying 43 items.
- Cystinosis (transclusion) (← links)
- Von Hippel-Lindau disease (transclusion) (← links)
- Arginemia (transclusion) (← links)
- Vitelliform macular dystrophy (transclusion) (← links)
- Leber's hereditary optic neuropathy (transclusion) (← links)
- Bloom syndrome (transclusion) (← links)
- 3-Methylcrotonyl-CoA carboxylase deficiency (transclusion) (← links)
- 3-Methylglutaconic aciduria (transclusion) (← links)
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (transclusion) (← links)
- Carbamoyl phosphate synthetase I deficiency (transclusion) (← links)
- Duane-radial ray syndrome (transclusion) (← links)
- Emery-Dreifuss muscular dystrophy (transclusion) (← links)
- Ethylmalonic encephalopathy (transclusion) (← links)
- Fabry's disease (transclusion) (← links)
- Glutaric aciduria type 1 (transclusion) (← links)
- Glutathione synthetase deficiency (transclusion) (← links)
- Greig cephalopolysyndactyly syndrome (transclusion) (← links)
- Hereditary coproporphyria (transclusion) (← links)
- Holt-Oram syndrome (transclusion) (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (transclusion) (← links)
- Isovaleric acidemia (transclusion) (← links)
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (transclusion) (← links)
- Malonyl-CoA decarboxylase deficiency (transclusion) (← links)
- Maple syrup urine disease (transclusion) (← links)
- Medium-chain acyl-coenzyme A dehydrogenase deficiency (transclusion) (← links)
- Mitochondrial trifunctional protein deficiency (transclusion) (← links)
- Myotonic dystrophy (transclusion) (← links)
- Neuropathy, ataxia, and retinitis pigmentosa (transclusion) (← links)
- Ornithine translocase deficiency (transclusion) (← links)
- Pallister-Hall syndrome (transclusion) (← links)
- Pyruvate carboxylase deficiency (transclusion) (← links)
- Short-chain acyl-coenzyme A dehydrogenase deficiency (transclusion) (← links)
- Spondyloepiphyseal dysplasia congenita (transclusion) (← links)
- Spondyloperipheral dysplasia (transclusion) (← links)
- Tay-Sachs disease (transclusion) (← links)
- Very long-chain acyl-coenzyme A dehydrogenase deficiency (transclusion) (← links)
- Perforin (transclusion) (← links)
- Methylmalonic acidemia (transclusion) (← links)
- Hearing loss with craniofacial syndromes (transclusion) (← links)
- Erythropoietic protoporphyria (transclusion) (← links)
- Methylmalonyl-CoA mutase deficiency (transclusion) (← links)
- Hepatoerythropoietic porphyria (transclusion) (← links)
- Argininemia (transclusion) (← links)