Conditions and Diseases -- Birth Defects
4
A
- Aarskog-Scott syndrome
- AAT deficiency
- Abdominal hernia
- Abdominal wall defect
- Achondroplasia
- Achondroplastic dwarfism
- Acute central cord syndrome
- Adrenoleukodystrophy X-linked
- Aganglionic megacolon
- Agranulocytosis
- Albinism
- Alcohol in pregnancy
- Alpha 1 anti-trypsin deficiency
- Alpha-1 antiprotease deficiency
- ALS
- Alpha-galactosidase A deficiency
- Amyotrophic lateral sclerosis
- AN
- Anal atresia
- Anderson-Fabry disease
- Angiokeratoma corporis diffusum
- Angiokeratoma diffuse
- Anomia, aphasia-associated
- Anomic aphasia
- Anorectal malfunction
- Anthrax
- Aphasia-associated anomia
- Arnold-Chiari malformation
- Arnold-Chiari syndrome
- Arteriovenous malformations
- ASD
- Atrial septal defect
- Auditory dyssynchrony
- Auditory neuropathy
- Auditory processing disorder
- Auditory synaptopothy
- AVM
B
C
- CCS
- Central cervical cord syndrome
- Central cord injury
- Central cord syndrome
- Ceramide trihexosidase deficiency
- Cerebellomedullary malformation syndrome
- Cervical myelopathy
- Chromosome 22q11 deletion syndrome
- Cleft lip
- Cleft palate
- Colonic aganglionosis
- Congenital dislocation of the hip
- Congenital dysplasia of the hip
- Congenital dysplasia/dislocation of the hip [CDH]
- Congenital hernia of the diaphragm
- Congenital hip dislocation
- Congenital hip dysplasia
- Congenital hip subluxability
- Congenital kyphosis
- Congenital megacolon or megarectum
- Congenital rubella syndrome
- Congenital subluxability of the hip
- Copper transport disease
- Craniofacial dysotosis
- Crouzon syndrome
- CRS
- Cryptorchidism
- Cystic fibrosis
D
- D incompatibility
- Dandy Walker
- Dandy Walker malformation
- Dandy-Walker syndrome
- DDH
- Developmental dysplasia of the hip
- Deviated nasal septum
- Diaphragmatic hernia
- Difficulty naming objects and people
- DiGeorge syndrome
- DMD
- Down's syndrome
- Drinking alcohol during pregnancy
- Duchenne muscular dystrophy
- Dysplasia of the hip, developmental
E
- Early-onset germinal matrix hemorrhage
- EDS
- EGMH
- Ehlers-Danlos syndrome
- Epigastic hernia
- Erb's palsy
- Erb-duchenne paralysis
F
- Fabry disease
- Faciodigitogenital dysplasia
- Familial adenomatous polyposis
- Familial Dandy Walker
- Familial hypercholesterolemia
- Fecal incontinence
- Femoral hernia
- FH
G
H
- Hemangioma
- Hemophilia
- Hereditary dystopic lipidosis
- Hernia, abdominal
- Hernia—diaphragmatic
- Hiatal hernia
- Hirschprung-Galant infantilism
- Hirschsprung's disease
- Hole in the heart
- Hunchback
- Huntington's chorea
- Huntington's disease
I
- Ichthyosis
- Imperforate anus
- Incisional hernia
- Infantile hypertrophic pyloric stenosis
- Inguinal hernia
- Injury, central cord
- Intraventricular hemorrhage of infancy
- IVH
K
L
M
- Marfan syndrome
- Martin-Bell syndrome
- Meckel's diverticulum
- Menkes syndrome
- Mya's disease
- Myelopathy, cervical
N
- Neural tube defect – spina bifida
- Neurofibromatosis
- Neuronal ceroid lipofuscinoses
- Neuropathy, auditory
- Neutropenia
- Niemann-Pick disease
- Nominal aphasia
O
P
- Paralysis, upper extremity
- Periventricular-intraventricular hemorrhage
- Persistent pulmonary hypertension of the newborn
- PIVH
- Postural kyphosis
- PPHN
- Prader-Willi syndrome
- Primary lymphedema
- Pseudohypertrophic muscular dystophy
- Pyloric stenosis
R
S
- Scheuermann's kyphosis
- Schilder’s disease
- Seconary lymphedema
- Septal defects
- SHE
- Sickle cell anemia
- Sickle cell disease
- Sinus headache
- Spigelian hernia
- Spina bifida
- Steely hair disease
- Subependymal germinal matrix hemorrhage
- Sudanophilic leukodystrophy
- Syndrome, central cervical cord
- Syndrome, central cord
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
- Velocardiofacial syndrome
- Ventral hernia
- Ventricular septal defect
- Von Hippel-Lindau disease
- Von Willebrand disease
W
X
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