Category:Genetic disorders

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fr:Catégorie:Maladie génétique

nl:Categorie:Erfelijke aandoening pl:Kategoria:Choroby genetyczne

Subcategories

There is 1 subcategory to this category.

C

• Congenital genetic disorders

Articles in category "Genetic disorders"

There are 129 articles in this category.

* List of genetic disorders 3 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-methylcrotonyl-CoA carboxylase deficiency A Aarskog syndrome Aase syndrome Abderhalden-Kaufmann-Lignac syndrome Abetalipoproteinemia Achondroplasia Acrofacial dysostosis, Nager type Adducted thumb syndrome recessive form Adenosine deaminase deficiency Alkaptonuria Alpha 1-antitrypsin deficiency Alpha-mannosidosis Alport syndrome Andersen-Tawil syndrome Androgen insensitivity syndrome Aneuploidy Anticipation (genetics) Apert syndrome Ataxia telangiectasia B Bardet-Biedl syndrome Barth syndrome Becker's muscular dystrophy Beta-ketothiolase deficiency Birt-Hogg-Dubé syndrome Bloom syndrome Brugada syndrome C Canavan disease Cerebral cavernous malformations Charcot-Marie-Tooth disease Chromosome 22, microdeletion 22 q11 Chronic granulomatous disease Citrullinemia Cockayne syndrome Coffin-Lowry syndrome Congenital adrenal hyperplasia Cri du chat Crouzon syndrome D DiGeorge syndrome Dor Yeshorim Duchenne muscular dystrophy E Ellis-van Creveld syndrome

E cont. Epidermolytic hyperkeratosis F Familial Mediterranean fever Familial adenomatous polyposis Familial dysautonomia Fanconi anemia Fragile X syndrome Fructose intolerance Fructose malabsorption G Galactosemia Gaucher's disease Genetic disorder Gitelman syndrome Glanzmann's thrombasthenia H Haemochromatosis Haemophilia Harlequin type ichthyosis Hereditary hemorrhagic telangiectasia Hereditary nonpolyposis colorectal cancer Hereditary spastic paraplegia Holocarboxylase synthetase deficiency Homocystinuria Howel-Evans syndrome Human genetics Hurler syndrome Hyperimmunoglobinemia D with recurrent fever I Ichthyosis Ichthyosis vulgaris Immunodeficiency, centromere instability and facial anomalies syndrome Isovaleric acidemia J Jervell and Lange-Nielsen syndrome Joubert syndrome K Klinefelter's syndrome L Leber's hereditary optic neuropathy Lesch-Nyhan syndrome Li-Fraumeni syndrome Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency M MOMO syndrome Maple syrup urine disease Marfan syndrome Medium chain acyl dehydrogenase deficiency Mitochondrial disease Mulibrey nanism Myeloperoxidase deficiency N Neurofibromatosis

N cont. Neurofibromatosis type I Norrie disease O Occipital horn syndrome Osteogenesis imperfecta P Pendred syndrome Peutz-Jeghers syndrome Phenylketonuria Polycystic kidney disease Porphyria Preimplantation genetic diagnosis Primary carnitine deficiency Progeria Propionic acidemia R Retinitis pigmentosa Romano-Ward syndrome Rothmund-Thompson's syndrome Rubinstein-Taybi syndrome S Schamberg disease pigmentation disorder Sickle cell anemia Smith-Lemli-Opitz syndrome Stickler syndrome T TAR syndrome Tay-Sachs disease Thalassemia Timothy syndrome Treacher Collins syndrome Trimethylaminuria Triple X syndrome Tuberous scelerosis Tuberous sclerosis Turner syndrome Tyrosinemia V Von Gierke's disease Von Willebrand disease W Waardenburg syndrome Weissenbacher-Zweymuller syndrome Werner syndrome Williams syndrome Wilson's disease Wiskott-Aldrich syndrome X X-linked ichthyosis Xeroderma pigmentosum

Wikipedia (http://en.wikipedia.org/wiki/Main_Page) Category:Genetic_disorders (http://en.wikipedia.org/wiki/Category:Genetic_disorders) version history (http://en.wikipedia.org/w/index.php?title=Category:Genetic_disorders&action=history) GNU Free Documentation Lizenz (http://en.wikipedia.org/wiki/Wikipedia:Text_of_the_GNU_Free_Documentation_License) CC-by-sa (http://creativecommons.org/licenses/by-sa/2.5/)

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