Category:Hereditary/congenital
Pages in category "Hereditary/congenital"
The following 87 pages are in this category, out of 87 total.
A
- Achondroplasia (acrondroplastic dwarfism)
- Adrenal gland disorder, NOS
- Albinism (albino)
- Alopecia (nonscarring hair loss)
- Alpha-1 antitrypsin deficiency
- Anemia, due to enzyme disorders
- Aortic valve or mitral valve, congenital malformation
- Arteriovenous malformation (AVM)
- Arteriovenous malformation (AVM) of cerebral vessels
- Atrial septal defect (ASD), congenital
C
D
- Digestive system, congenital malformation
- Disorder of bilirubin metabolism
- Disorder of carbohydrate metabolism
- Disorder of copper metabolism
- Disorder of glycosaminoglycan metabolism
- Disorder of lipoprotein metabolism NOS
- Disorder of purine and pyrimidine metabolism
- Disorder of sphingolipid metabolism, and other lipid storage disorders
- Disorder of the newborn originating in perinatal period (applies to baby, not mom)
- Down syndrome (trisomy 21)
F
H
- Heart NOS, congenital malformation
- Hemochromatosis
- Hemoglobinopathy, hereditary, NOS
- Hereditary coagulation factor IX deficiency (Christmas disease, hemophilia B)
- Hereditary coagulation factor VIII deficiency (classic hemophilia A)
- Hereditary deficiency of clotting factor, NOS
- Hermaphroditism, pseudohermaphroditism
- Huntington's disease/chorea
- Hyperphosphatemia, hypophosphotemia or other disorder of phosphate metabolism, severe or symptomatic
- Hypocalcemia, severe or symptomatic
M
- Male genital organs NOS, congenital malformation
- Malformation/disorder NOS, congenital
- Malformation/dysmorphism due to substances taken by mother, NOS, congenital (applies to baby, not mom)
- Marfan syndrome
- Maternal disorder complicating pregnancy, childbirth, or postpartum, NOS
- Mitral valve disorder, NOS
- Multiple endocrine adenomatosis (multiple endocrine neoplasia syndrome, MEN)
- Myotonic dystrophy, all types