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)