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Genetic Conditions…
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© 2006 Betterchem Corp.
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[Index] | [Continue]
- Lacunar Dementia see CADASIL
- Langer-Saldino achondrogenesis see achondrogenesis, type 2
- Langer-Saldino dysplasia see achondrogenesis, type 2
- Late Onset Alzheimer Disease see Alzheimer disease, type 2
- Late-Onset Familial Alzheimer Disease (AD2) see Alzheimer disease, type 2
- late-onset Krabbe disease (LOKD) see Krabbe disease
- LCHAD deficiency see long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
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Learning Disorders
- Lentiginosis, Perioral see Peutz-Jeghers syndrome
- Lesch-Nyhan syndrome
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Leukodystrophies
- Leukodystrophy, spongiform see Canavan disease
- leukodystrophy with Rosenthal fibers see Alexander disease
- Lewy Body Disease see Parkinson disease
- LFS see Li-Fraumeni syndrome
- Li-Fraumeni syndrome
- Lipase D deficiency see familial lipoprotein lipase deficiency
- LIPD deficiency see familial lipoprotein lipase deficiency
- Lipidosis, cerebroside see Gaucher disease
- Lipidosis, ganglioside, infantile see Tay-Sachs disease
- lipoid histiocytosis (classical phosphatide) see Niemann-Pick disease
- Lipoid histiocytosis (kerasin type) see Gaucher disease
- Lipoprotein Lipase Deficiency, Familial see familial lipoprotein lipase deficiency
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Liver Diseases
- LNS see Lesch-Nyhan syndrome
- long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- Long QT Syndrome 1 see Romano-Ward syndrome
- Long QT syndrome 7 see Andersen-Tawil syndrome
- Lou Gehrig Disease see amyotrophic lateral sclerosis
- Louis-Bar syndrome see ataxia-telangiectasia
- LQT7 see Andersen-Tawil syndrome
- Lynch Syndrome see hereditary nonpolyposis colorectal cancer
- Lysyl-hydroxylase deficiency see Ehlers-Danlos syndrome, kyphoscoliosis type
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