2022 ICD-10-CM Diagnosis Code G60.0 · Hereditary motor and sensory neuropathy · Diseases of the nervous system · Polyneuropathies and other disorders of the ...
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G60.0 - Hereditary motor and sensory neuropathy answers are found in the ICD-10-CM powered by Unbound Medicine. Available for iPhone, iPad, Android, ...
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G60.0 Hereditary motor and sensory neuropathy. Incl.: Disease: Charcot-Marie-Tooth; Déjerine-Sottas. Hereditary motor and sensory neuropathy, ...
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Charcot-Marie-Tooth Disease G60.0 356.1 · present 1-3 decade, +family hx · slowly progressive distal muscular weakness and atrophy with minor deficits in ... ICD-9 · Classification / Treatment
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ICD-10 code G60.0 for Hereditary motor and sensory neuropathy is a medical classification as listed by WHO under the range -Polyneuropathies and other.
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G60.0 is a billable diagnosis code used to specify a medical diagnosis of hereditary motor and sensory neuropathy. Code valid for the fiscal year 2022.
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42 Type 2 diabetes mellitus with diabetic polyneuropathy. Refer to ACS 0401 Rule 4b to determine if the additional diagnosis of G60.0 Hereditary motor and ...
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Synonym(s):. CMTDID. Prevalence:
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ORPHA:100044 · Synonym(s):. CMTDIB · Prevalence:
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Disease name: Charcot-Marie-Tooth disease ICD 10: G60.0 Synonyms: Hereditary motor and sensory neuropathy. Includes: Charcot-Marie-Tooth, Déjerine-Sottas, ...
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16 thg 2, 2021 · Notes: aDiagnostic codes ICD-8 35401, ICD-10 G60.3, G60.8, G60.9, G62.8 and G62.9; b516 CMT diagnoses and 3 Refsum disease diagnoses; ...
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16 thg 2, 2021 · Notes:aDiagnostic codes ICD-8 35401, ICD-10 G60.3, G60.8, G60.9, ... with a CMT diagnosis (ICD-10 DG60.0 Hereditary motor and sensory ...
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CMT is diagnosed in individuals with a clinical presentation, including toe-walking or foot abnormalities ... G60.0, Hereditary motor and sensory neuropathy ...
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Alt IDs: OMIM:310490, ICD10CM:G60.0, ORDO:101078 ... Charcot-Marie-Tooth disease type X + is-a ... Charcot-Marie-Tooth disease X-linked recessive 4.
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Alt IDs: OMIM:118200, ICD10CM:G60.0, ORDO:101082 ; Definition: A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the gene ...
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