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Table of Contents
1
Numerical
2
A
3
B
4
C
5
D
6
E
7
F
8
G
9
H
10
I
11
J
12
K
13
L
14
M
15
N
16
O
17
P
18
R
19
S
20
T
21
U
22
W
23
See also
Categories
Congenital disorders
List of congenital disorders
Topic: Medicine
From
HandWiki
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Short description
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List of congenital disorders
Contents
1
Numerical
2
A
3
B
4
C
5
D
6
E
7
F
8
G
9
H
10
I
11
J
12
K
13
L
14
M
15
N
16
O
17
P
18
R
19
S
20
T
21
U
22
W
23
See also
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
Rare disease
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