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ICD-10-CM

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N07.B — Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]

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N07.0 — Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality

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N07.1 — Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions

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N07.2 — Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis

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N07.3 — Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis

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N07.4 — Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis

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N07.5 — Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis

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N07.6 — Hereditary nephropathy, not elsewhere classified with dense deposit disease

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N07.7 — Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis

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N07.8 — Hereditary nephropathy, not elsewhere classified with other morphologic lesions

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N07.9 — Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions

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N07.A — Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis

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N07 — Hereditary nephropathy, not elsewhere classified

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G60 — Hereditary and idiopathic neuropathy

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G60.9 — Hereditary and idiopathic neuropathy, unspecified

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G60.2 — Neuropathy in association with hereditary ataxia

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G60.0 — Hereditary motor and sensory neuropathy

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D66 — Hereditary factor VIII deficiency

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D67 — Hereditary factor IX deficiency

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G11 — Hereditary ataxia

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D56.4 — Hereditary persistence of fetal hemoglobin [HPFH]

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D58 — Other hereditary hemolytic anemias

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D58.0 — Hereditary spherocytosis

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D58.1 — Hereditary elliptocytosis

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D58.8 — Other specified hereditary hemolytic anemias

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D58.9 — Hereditary hemolytic anemia, unspecified

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D59.32 — Hereditary hemolytic-uremic syndrome

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D64.0 — Hereditary sideroblastic anemia

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D68.1 — Hereditary factor XI deficiency

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D68.2 — Hereditary deficiency of other clotting factors

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D69.42 — Congenital and hereditary thrombocytopenia purpura

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D80.0 — Hereditary hypogammaglobulinemia

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D82.3 — Immunodeficiency following hereditary defective response to Epstein-Barr virus

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D89.44 — Hereditary alpha tryptasemia

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E74.12 — Hereditary fructose intolerance

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E79.82 — Hereditary xanthinuria

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E80.0 — Hereditary erythropoietic porphyria

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E83.110 — Hereditary hemochromatosis

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E83.32 — Hereditary vitamin D-dependent rickets (type 1) (type 2)

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G11.4 — Hereditary spastic paraplegia

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G11.8 — Other hereditary ataxias

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G11.9 — Hereditary ataxia, unspecified

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G60.8 — Other hereditary and idiopathic neuropathies

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H18.5 — Hereditary corneal dystrophies

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H18.50 — Unspecified hereditary corneal dystrophies

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H18.501 — Unspecified hereditary corneal dystrophies, right eye

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H18.502 — Unspecified hereditary corneal dystrophies, left eye

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H18.503 — Unspecified hereditary corneal dystrophies, bilateral

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H18.509 — Unspecified hereditary corneal dystrophies, unspecified eye

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H18.59 — Other hereditary corneal dystrophies

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H18.591 — Other hereditary corneal dystrophies, right eye

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H18.592 — Other hereditary corneal dystrophies, left eye

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H18.593 — Other hereditary corneal dystrophies, bilateral

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H18.599 — Other hereditary corneal dystrophies, unspecified eye

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H31.2 — Hereditary choroidal dystrophy

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H31.20 — Hereditary choroidal dystrophy, unspecified

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H31.29 — Other hereditary choroidal dystrophy

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H35.5 — Hereditary retinal dystrophy

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H35.50 — Unspecified hereditary retinal dystrophy

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H47.22 — Hereditary optic atrophy