
2006 ICD-9-CM Diagnosis Code 655.20
Hereditary disease in family possibly affecting fetus affecting management of mother unspecified as to episode of care in pregnancy
- Short description: FAMIL HEREDIT DIS-UNSPEC.
- ICD-9-CM 655.20 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 655.20 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
- You are viewing the 2006 version of ICD-9-CM 655.20.
- More recent version(s) of ICD-9-CM 655.20: 2007 2008 2009 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM:
655.20 converts approximately to:
- 2015/16 ICD-10-CM O35.2XX0 Maternal care for (suspected) hereditary disease in fetus, not applicable or unspecified
Approximate Synonyms
- Charcot-Marie-Tooth disease, fetus affected
- Dystrophy, muscular, duchenne, fetus affected
- Familial dysautonomia, fetus
- Familial hypertriglyceridemia, fetus affected
- Fetal alpha thalassemia
- Fetal alpha thalassemia. (disorder)
- Fetal beta thalassemia
- Fetal canavan disease
- Fetal Charcot-Marie-Tooth disease
- Fetal cystic fibrosis
- Fetal duchenne muscular dystrophy
- Fetal familial combined hyperlipidemia
- Fetal familial dysautonomia
- Fetal familial hyperbetalipoproteinemia
- Fetal familial hypercholesterolemia
- Fetal familial hypertriglyceridemia
- Fetal familial hypoalphalipoproteinemia
- Fetal genetic cancer
- Fetal hemochromatosis
- Fetal hemoglobinopathy
- Fetal hemoglobinopathy C
- Fetal hemoglobinopathy E
- Fetal hemophilia
- Fetal hereditary disease
- Fetal hereditary hemochromatosis
- Fetal huntington disease
- Fetal lysosomal storage disease
- Fetal Marfan syndrome
- Fetal mitochondrial defect
- Fetal myotonic muscular dystrophy
- Fetal neurogenetic disorder
- Fetal polycystic kidney disease
- Fetal sickle cell anemia
- Fetal Tay-Sachs disease
- Fetal von Willebrand disease
- Fetus with hereditary disease
- Hereditary hemochromatosis, fetus affected
- Myotonic muscular dystrophy, fetus affected
- Tay-Sachs disease in fetus
- von Willebrand disorder in fetus