Category:Genetic disorders patient information: Difference between revisions
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Latest revision as of 14:22, 27 July 2011
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Pages in category "Genetic disorders patient information"
The following 68 pages are in this category, out of 68 total.
A
- Aarskog-Scott syndrome (patient information)
- Achondroplasia (patient information)
- Adrenoleukodystrophy (patient information)
- Alagille syndrome (patient information)
- Alkaptonuria (patient information)
- Alpha 1-antitrypsin deficiency (patient information)
- Amblyopia (patient information)
- Amyotrophic lateral sclerosis (patient information)
- Ataxia (patient information)
- Ataxia telangiectasia (patient information)
C
- Canavan disease (patient information)
- Celiac disease (patient information)
- Cerebral palsy (patient information)
- Color blindness (patient information)
- Congenital hypothyroidism (patient information)
- Congenital protein C or S deficiency (patient information)
- Costello syndrome (patient information)
- Craniosynostosis (patient information)
- Cri du chat (patient information)
- Crigler-Najjar syndrome (patient information)
G
H
M
P
- Paroxysmal nocturnal hemoglobinuria (patient information)
- Patau syndrome (patient information)
- Template:Patient information page
- Pericardial effusion (patient information)
- Phenylketonuria (patient information)
- Phosphate nephropathy (patient information)
- Polycystic kidney disease (patient information)
- Post-streptococcal glomerulonephritis (patient information)
- Prader-Willi syndrome (patient information)
- Pyonephrosis (patient information)