O35.2XX0

ICD-10-CM Coding Rules

• O35.2XX0

• O35.2XX0

Approximate Synonyms

• Charcot-marie-tooth disease, fetus affected

• Connective tissue disorder, fetus affected

• Dystrophy, muscular, duchenne, fetus affected

• Familial dysautonomia, fetus

• Familial hypertriglyceridemia, fetus affected

• Fetal achondroplasia

• Fetal alpha thalassemia

• Fetal beta thalassemia

• Fetal canavan disease

• Fetal charcot-marie-tooth disease

• Fetal connective tissue disorder

• 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 finnish nephrosis

• Fetal fragile x syndrome

• Fetal galactosemia

• Fetal genetic cancer

• Fetal glycogen storage disease

• Fetal hemochromatosis

• Fetal hemoglobinopathy

• Fetal hemoglobinopathy c

• Fetal hemoglobinopathy e

• Fetal hemophilia

• Fetal hereditary disease

• Fetal hereditary hemochromatosis

• Fetal hereditary hemochromatosis disorder)

• Fetal huntington disease

• Fetal lysosomal storage disease

• Fetal marfan syndrome

• Fetal methylmalonic acidemia

• Fetal mitochondrial defect

• Fetal myotonic muscular dystrophy

• Fetal neurofibromatosis

• Fetal neurogenetic disorder

• Fetal phenylketonuria

• Fetal polycystic kidney disease

• Fetal propionic acidemia

• Fetal sickle cell anemia

• Fetal skeletal dysplasia

• Fetal spinocerebellar ataxia

• Fetal tay-sachs disease

• Fetal von willebrand disease

• Fetus with hereditary disease

• Hereditary disease in family possibly affecting fetus

• Hereditary hemochromatosis, fetus affected

• Myotonic muscular dystrophy, fetus affected

• Spinocerebellar ataxia in fetus

• Tay-sachs disease in fetus

• Von willebrand disorder in fetus

Details

• O35.2XX0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• Short description: Maternal care for hereditary disease in fetus, unsp

• The 2023 edition of ICD-10-CM O35.2XX0 became effective on October 1, 2022.

• This is the American ICD-10-CM version of O35.2XX0 – other international versions of ICD-10 O35.2XX0 may differ.