Hereditary ICD-10 Code

• G11.9 - Hereditary ataxia, unspecified
• O35.2 - Maternal care for (suspected) hereditary disease in fetus
• D64.0 - Hereditary sideroblastic anemia
• G11.8 - Other hereditary ataxias
• G11.9 - Hereditary ataxia, unspecified
• G11.11 - Friedreich ataxia
• G11.4 - Hereditary spastic paraplegia
• H18.5 - Hereditary corneal dystrophies
• H18.50 - Unspecified hereditary corneal dystrophies
• H18.501 - Unspecified hereditary corneal dystrophies, right eye
• H18.502 - Unspecified hereditary corneal dystrophies, left eye
• H18.509 - Unspecified hereditary corneal dystrophies, unspecified eye
• H18.59 - Other hereditary corneal dystrophies
• H18.591 - Other hereditary corneal dystrophies, right eye
• H18.592 - Other hereditary corneal dystrophies, left eye
• H18.599 - Other hereditary corneal dystrophies, unspecified eye
• H18.503 - Unspecified hereditary corneal dystrophies, bilateral
• H18.593 - Other hereditary corneal dystrophies, bilateral
• H18.54 - Lattice corneal dystrophy
• G11.3 - Cerebellar ataxia with defective DNA repair
• I67.85 - Hereditary cerebrovascular diseases
• I67.858 - Other hereditary cerebrovascular disease
• I67.858 - Other hereditary cerebrovascular disease
• I67.85 - Hereditary cerebrovascular diseases
• H31.20 - Hereditary choroidal dystrophy, unspecified
• H31.2 - Hereditary choroidal dystrophy
• H31.29 - Other hereditary choroidal dystrophy
• G11.0 - Congenital nonprogressive ataxia
• H18.501 - Unspecified hereditary corneal dystrophies, right eye
• H18.502 - Unspecified hereditary corneal dystrophies, left eye
• H18.509 - Unspecified hereditary corneal dystrophies, unspecified eye
• H18.591 - Other hereditary corneal dystrophies, right eye
• H18.592 - Other hereditary corneal dystrophies, left eye
• H18.599 - Other hereditary corneal dystrophies, unspecified eye
• N07.6 - Hereditary nephropathy, not elsewhere classified with dense deposit disease
• N07.4 - Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
• N07.3 - Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
• O35.2 - Maternal care for (suspected) hereditary disease in fetus
• D58.1 - Hereditary elliptocytosis
• H18.51 - Endothelial corneal dystrophy
• E80.0 - Hereditary erythropoietic porphyria
• D68.2 - Hereditary deficiency of other clotting factors
• E74.12 - Hereditary fructose intolerance
• N07.A - Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis
• N07.A - Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis
• E83.110 - Hereditary hemochromatosis
• D56.4 - Hereditary persistence of fetal hemoglobin [HPFH]
• D58.9 - Hereditary hemolytic anemia, unspecified
• D58.8 - Other specified hereditary hemolytic anemias
• D80.0 - Hereditary hypogammaglobulinemia
• G60.9 - Hereditary and idiopathic neuropathy, unspecified
• G60.8 - Other hereditary and idiopathic neuropathies
• Q82.0 - Hereditary lymphedema
• Q82.0 - Hereditary lymphedema
• D69.42 - Congenital and hereditary thrombocytopenia purpura
• D68.1 - Hereditary factor XI deficiency
• D58.1 - Hereditary elliptocytosis
• D58.2 - Other hemoglobinopathies
• D58.8 - Other specified hereditary hemolytic anemias
• D58.0 - Hereditary spherocytosis
• D80.0 - Hereditary hypogammaglobulinemia
• D82.3 - Immunodeficiency following hereditary defective response to Epstein-Barr virus
• N07.2 - Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis
• N07.5 - Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
• N07.8 - Hereditary nephropathy, not elsewhere classified with other morphologic lesions
• N07.9 - Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions
• N07.8 - Hereditary nephropathy, not elsewhere classified with other morphologic lesions
• N07.9 - Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions
• N07.0 - Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality
• E74.12 - Hereditary fructose intolerance
• E79.82 - Hereditary xanthinuria
• E80.0 - Hereditary erythropoietic porphyria
• H47.22 - Hereditary optic atrophy
• G11.4 - Hereditary spastic paraplegia
• G60.8 - Other hereditary and idiopathic neuropathies
• G60.9 - Hereditary and idiopathic neuropathy, unspecified
• G60.3 - Idiopathic progressive neuropathy
• D69.42 - Congenital and hereditary thrombocytopenia purpura
• H35.5 - Hereditary retinal dystrophy
• H35.50 - Unspecified hereditary retinal dystrophy
• N07.1 - Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
• D58.0 - Hereditary spherocytosis
• D59.32 - Hereditary hemolytic-uremic syndrome
• I78.0 - Hereditary hemorrhagic telangiectasia
• K00.5 - Hereditary disturbances in tooth structure, not elsewhere classified
• D89.44 - Hereditary alpha tryptasemia
• E83.32 - Hereditary vitamin D-dependent rickets (type 1) (type 2)