Conditions and Diseases -- Birth Defects
This collection focuses on conditions associated to birth defects. Many of these conditions are aligned to the ICD-9 codes 740-759.
These comprehensive and concise factsheets are physician-reviewed and reflect the most current, evidence-based information. Relevant sources are provided for each fact sheet.
A
- Aarskog-Scott syndrome
- Achondroplasia
- Achondroplastic dwarfism
- Adrenoleukodystrophy (X-linked)
- Aganglionic megacolon
- Agranulocytosis
- Albinism
- Alpha-galactosidase A deficiency
- Amyotrophic lateral sclerosis (ALS)
- Anal atresia
- Anderson-Fabry disease
- Angiokeratoma corporis diffusum
- Angiokeratoma diffuse
- Anorectal malfuntion
- Anthrax
- Arnold-Chiari Malformation
- Arnold-Chiari Syndrome
- Arteriovenous malformations
- ASD
- Atrial septal defect
- AVM
B
C
- Ceramide trihexosidase deficiency
- Cerebellomedullary Malformation Syndrome
- Chromosome 22q11 deletion syndrome
- Cleft lip
- Cleft palate
- Colonic aganglionosis
- Congenital hernia of the diaphragm
- Congenital megacolon or megarectum
- Congenital rubella syndrome
- Copper transport disease
- Craniofacial dysotosis
- Crouzon syndrome
- Cryptorchidism
- Cystic fibrosis
D
- D incompatibility
- Dandy Walker
- Dandy Walker Malformation
- Dandy-Walker Syndrome
- Deviated nasal septum
- Diaphragmatic hernia
- DiGeorge syndrome
- Down's syndrome
E
F
G
H
- Hemangioma
- Hemophilia
- Hereditary dystopic lipidosis
- Hernia—diaphragmatic
- Hirschprung-Galant infantilism
- Hirschsprung's disease
- Hole in the heart
- Huntington's disease (Huntington's chorea)
I
K
M
N
- Neural tube defect – Spina bifida
- Neurofibromatosis
- Neuronal ceroid lipofuscinoses
- Neutropenia
- Niemann-Pick disease
O
P
R
S
- Schilder’s disease
- Septal defects
- Sickle cell anemia (Sickle cell disease)
- Sinus headache
- Spina bifida
- Steely hair disease
- Sudanophilic leukodystrophy
T
- Tay-Sachs disease
- Tetralogy of Fallot
- Trichopoliodystrophy
- Tricuspid regurgitation
- Tricuspid stenosis
- Tricuspid valve disease
- Trisomy 21
- Turner syndrome
- Type II Chiari Malformation
U
V
W
X
