List of congenital disorders

List of

Numerical

• 5p syndrome - see Cri du chat syndrome

A

• Acrorenal mandibular syndrome
• Albinism
• Amelia and hemimelia
• Amniotic band syndrome
• Anencephaly
• Angelman syndrome
• Aposthia
• Arnold–Chiari malformation

B

• Bannayan–Zonana syndrome
• Bardet–Biedl syndrome
• Barth syndrome
• Basal-cell nevus syndrome
• Beckwith–Wiedemann syndrome
• Benjamin syndrome
• Bladder exstrophy
• Bloom syndrome
• Brachydactyly

C

• Cat eye syndrome
• Caudal regression syndrome
• Sotos syndrome
  Cerebral Gigantism
• CHARGE syndrome
• Chromosome 16
  abnormalities
• Chromosome 18
  abnormalities
• Chromosome 20
  abnormalities
• Chromosome 22
  abnormalities
• Cleft lip/palate
• Cleidocranial dysostosis
• Club foot
• Congenital adrenal hyperplasia (CAH)
• Congenital central hypoventilation syndrome
• Congenital diaphragmatic hernia (CDH)
• Congenital Disorder of Glycosylation (CDG)
• Congenital hyperinsulinism
• Congenital insensitivity to pain with anhidrosis (CIPA)
• Congenital pulmonary airway malformation (CPAM)
• Conjoined twins
• Costello syndrome
• Craniopagus parasiticus
• Cri du chat syndrome
• Cyclopia
• Cystic fibrosis

D

• De Lange syndrome
• Diphallia
• Distal trisomy 10q
• Down syndrome

E

• Ectodermal dysplasia
• Ectopia cordis
• Ectrodactyly
• Encephalocele

F

• Fetal alcohol syndrome
• Fetofetal transfusion
• First arch syndrome
• Freeman–Sheldon syndrome

G

• Gastroschisis
• Genu recurvatum
• Goldenhar syndrome

H

• Harlequin-type ichthyosis
• Heart disorders
  (Congenital heart defects)
• Hemifacial microsomia
• Holoprosencephaly
• Huntington's disease
• Hirschsprung's disease, or congenital aganglionic megacolon
• Hypertrichosis
• Hypoglossia
• Hypomelanism or hypomelanosis (albinism)
• Hypospadias
• Haemophilia
• Heterochromia
• Hemochromatosis

I

• Imperforate anus
• Imperforate hymen
• Incontinentia pigmenti
• Intestinal neuronal dysplasia
• Ivemark syndrome

J

• Jacobsen syndrome

K

• Katz syndrome
• Klinefelter syndrome
• Kabuki syndrome
• Kyphosis

L

• Larsen syndrome
• Laurence–Moon syndrome
• Lissencephaly
• Lordosis

M

• Macrocephaly
• Marfan syndrome
• Microcephaly
• Micromelia
• Microtia
• Monosomy 9p
• Myasthenic syndrome
• Myelokathexis

N

• Nager's Syndrome
• Nail–patella syndrome
• Neonatal jaundice
• Neurofibromatosis
• Neuronal ceroid lipofuscinosis
• Noonan syndrome
• Nystagmus

O

• Ochoa syndrome
• Oculocerebrorenal syndrome
• Oligodactyly

P

• Pallister–Killian syndrome
• Pectus excavatum
• Pectus carinatum
• Phocomelia
• Pierre Robin syndrome
• Poland syndrome
• Polydactyly
• Polymelia
• Polysyndactyly
• Prader–Willi syndrome
• Proteus syndrome
• Prune belly syndrome

R

• Radial aplasia
• Rett syndrome
• Robinow syndrome
• Rubinstein–Taybi syndrome

S

• Saethre–Chotzen syndrome
• Schizencephaly
• Scoliosis
• Sickle cell disease
• Sirenomelia
• Situs inversus
• Smith–Lemli–Opitz syndrome
• Smith–Magenis syndrome
• Spina bifida
• Stickler Syndrome
• Strabismus
• Sturge–Weber syndrome
• Symbrachydactyly
• Syndactyly
• Syphilis, congenital

T

• Teratoma
• Treacher Collins syndrome
• Trichothiodystrophy
• Triple-X syndrome
• Trisomy 13
• Trisomy 9
• Turner syndrome

U

• Umbilical hernia
• Usher syndrome

W

• Waardenburg syndrome
• Werner syndrome
• Wolf–Hirschhorn syndrome
• Wolff–Parkinson–White syndrome

See also

• ICD-10 Chapter Q: Congenital malformations, deformations and chromosomal abnormalities
• List of ICD-9 codes 740–759: congenital anomalies
• Rare disease