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Genetic Conditions…
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© 2006 Betterchem Corp.
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[Index] | [Continue]
- pantothenate kinase-associated neurodegeneration
- Parathyroid Disorders see multiple endocrine neoplasia type 1
- Parkinson disease
- Parkinson's Disease see Parkinson disease
- Patau syndrome
- PBGD deficiency see acute intermittent porphyria
- PCC deficiency see propionic acidemia
- PCT see porphyria cutanea tarda
- PD - Parkinson's disease see Parkinson disease
- PDM see myotonic dystrophy, type 2
- Pendred syndrome
- Periodic Disease see familial Mediterranean fever
- Periodic paralysis, potassium-sensitive cardiodysrhythmic type see Andersen-Tawil syndrome
- Periodic peritonitis see familial Mediterranean fever
- Periorificial lentiginosis syndrome see Peutz-Jeghers syndrome
- Peripheral Nerve Disorders see familial dysautonomia
- Peripheral Neurofibromatosis see neurofibromatosis 1
- Peroneal Muscular Atrophy see Charcot-Marie-Tooth disease
- peroxisomal alanine:glyoxylate aminotransferase deficiency see primary hyperoxaluria
- Peutz-Jeghers syndrome
- Pfeiffer syndrome
- Phenylalanine Hydroxylase Deficiency Disease see phenylketonuria
- phenylketonuria
- Pheochromocytoma see von Hippel-Lindau syndrome
- Pierre Robin syndrome with fetal chondrodysplasia see Weissenbacher-Zweymüller syndrome
- Pigmentary cirrhosis see hemochromatosis
- PJS see Peutz-Jeghers syndrome
- PKAN see pantothenate kinase-associated neurodegeneration
- PKD see polycystic kidney disease
- PKU see phenylketonuria
- PLSJ see juvenile primary lateral sclerosis
- Plumboporphyria see ALAD deficiency porphyria
- PMA see Charcot-Marie-Tooth disease
- polycystic kidney disease
- Polyposis coli see familial adenomatous polyposis
- Polyposis, hamartomatous intestinal see Peutz-Jeghers syndrome
- Polyposis, Intestinal, II see Peutz-Jeghers syndrome
- Polyps-and-spots syndrome see Peutz-Jeghers syndrome
- Porphobilinogen synthase deficiency see ALAD deficiency porphyria
- porphyria
- porphyrin disorder see porphyria
- PPH see primary pulmonary hypertension
- PPOX deficiency see variegate porphyria
- Prader-Labhart-Willi syndrome see Prader-Willi syndrome
- Prader-Willi syndrome
- Presenile and senile dementia see Alzheimer disease
- Primary Hemochromatosis see hemochromatosis
- primary hyperoxaluria
- primary hyperuricemia syndrome see Lesch-Nyhan syndrome
- primary lateral sclerosis, juvenile see juvenile primary lateral sclerosis
- Primary Parkinsonism see Parkinson disease
- primary pulmonary hypertension
- Primary Senile Degenerative Dementia see Alzheimer disease
- prion disease
- Procollagen type EDS VII, mutant see Ehlers-Danlos syndrome, arthrochalasia type
- Progeria see Hutchinson-Gilford progeria syndrome
- Progeria-Like Syndrome see Cockayne syndrome
- progeroid nanism see Cockayne syndrome
- Progressive Chorea, Chronic Hereditary (Huntington) see Huntington disease
- Progressive Muscular Atrophy see spinal muscular atrophy
- Progressively deforming osteogenesis imperfecta with normal sclerae see osteogenesis imperfecta, type III
- PROMM see myotonic dystrophy, type 2
- propionic acidemia
- propionyl-CoA carboxylase deficiency see propionic acidemia
- Protoporphyria see erythropoietic protoporphyria
- Protoporphyrinogen oxidase deficiency see variegate porphyria
- Proximal myotonic dystrophy see myotonic dystrophy, type 2
- Proximal myotonic myopathy see myotonic dystrophy, type 2
- pseudo-Gaucher disease
- pseudo-Ullrich-Turner syndrome see Noonan syndrome
- pseudoxanthoma elasticum
- psychosine lipidosis see Krabbe disease
- pulmonary arterial hypertension see primary pulmonary hypertension
- Pulmonary Hypertension see primary pulmonary hypertension
- PWS see Prader-Willi syndrome
- PXE - Pseudoxanthoma elasticum see pseudoxanthoma elasticum
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