Category:Congenital genetic disorders

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).

Articles in category "Congenital genetic disorders"

There are 27 articles in this category.

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

D Diastrophic dysplasia Down syndrome E Edward's syndrome H Hunter syndrome K Kabuki syndrome Kallmann's syndrome Klinefelter's syndrome L Lobster hand M Maghazaji syndrome N Niemann-Pick disease

N cont. Noonan syndrome P Patau syndrome Polydactyly Prader-Willi syndrome S Situs inversus T Thanatophoric dysplasia U Usher syndrome W Wolf-Hirschhorn syndrome