Category:Congenital genetic disorders

From Freepedia

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).

Subcategories

There is 1 subcategory to this category.

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• Muscular dystrophy

Articles in category "Congenital genetic disorders"

There are 35 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 Cystic fibrosis D Diastrophic dysplasia

D cont. Down syndrome E Edward's syndrome Epidermolysis bullosa H Haemophilia A Haemophilia B Haemophilia C 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 Wiskott-Aldrich syndrome Wolf-Hirschhorn syndrome X XYY syndrome