Congenital disorder
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).
See also
Reference
- The National Library of Medicine or MEDLINE/PubMed (medical subject heading) term
List of congenital disorders
- Aicardi Syndrome
- Amniotic Band Syndrome
- Anencephaly
- Angelman Syndrome
- Bannayan-Zonana Syndrome
- Barth Syndrome
- Basal Cell Nevus Syndrome
- Beckwith-Wiedemann Syndrome
- Bloom Syndrome
- Cat Eye Syndrome
- Cerebral Gigantism
- CHARGE Syndrome
- Chromosome 16 Abnormalities
- Chromosome 18 Abnormalities
- Chromosome 20 Abnormalities
- Chromosome 22 Abnormalities
- Costello Syndrome
- Cri-du-Chat Syndrome
- Cystic Fibrosis
- De Lange Syndrome
- Distal Trisomy 10q
- Down Syndrome
- Ectodermal Dysplasia
- Fetal Alcohol Syndrome
- Fetofetal Transfusion
- Freeman-Sheldon Syndrome
- Gastroschisis
- Holoprosencephaly
- Incontinentia Pigmenti
- Ivemark Syndrome
- Jacobsen Syndrome
- Klinefelter Syndrome
- Larsen Syndrome
- Laurence-Moon Syndrome
- Lissencephaly
- Microcephaly
- Monosomy 9p-
- Nail-Patella Syndrome
- Neonatal Jaundice
- Neurofibromatoses
- Neuronal Ceroid-Lipofuscinosis
- Noonan Syndrome
- Ochoa Syndrome
- Oculocerebrorenal Syndrome
- Pallister-Killian Syndrome
- Prader-Willi Syndrome
- Proteus Syndrome
- Prune Belly Syndrome
- Rett Syndrome
- Robinow Syndrome
- Rubinstein-Taybi Syndrome
- Schizencephaly
- Situs Inversus
- Smith-Lemli-Opitz Syndrome
- Smith-Magenis Syndrome
- Sturge-Weber Syndrome
- Syphilis, Congenital
- Trichothiodystrophy
- Triple-X Females
- Trisomy 13
- Trisomy 9
- Turner Syndrome
- Twins, Conjoined
- Umbilical Hernia
- Usher Syndrome
- Waardenburg's Syndrome
- Werner Syndrome
- Wolf-Hirschhorn Syndrome
