Category:Congenital genetic disorders

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A congenital disorder is a medical condition or defect that is present at or before birth (for example, congenital heart disease). These conditions can be a result of heredity or environmental factors - meaning a congenital condition could be acquired during the fetal stage of development, or as a result of the genetic make-up of the parents (or both).fr:Catégorie:Maladie génétique congénitale

Articles in category "Congenital genetic disorders"

There are 29 articles in this category.

A Aicardi syndrome Alagille syndrome Albinism Angelman syndrome Atelosteogenesis, type II C Chromosome 15q partial deletion Chromosome 15q trisomy Congenital insensitivity to pain with anhidrosis Craniopagus parasiticus

C cont. Cystic fibrosis D Diastrophic dysplasia Down syndrome E Edward's syndrome H Hexadactyly Hunter syndrome K Kabuki syndrome Klinefelter's syndrome L Langer-Giedion syndrome Lobster hand

M Maghazaji syndrome N Niemann-Pick disease Noonan syndrome P Patau syndrome Polydactyly Prader-Willi syndrome S Situs inversus T Thanatophoric dysplasia U Usher syndrome W Wolf-Hirschhorn syndrome

Wikipedia (http://en.wikipedia.org/wiki/Main_Page) Category:Congenital_genetic_disorders (http://en.wikipedia.org/wiki/Category:Congenital_genetic_disorders) version history (http://en.wikipedia.org/w/index.php?title=Category:Congenital_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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