DISORDERS OF THE PERIPHERAL NERVOUS SYSTEM (350-359)
- Excludes: diseases of:
- acoustic [8th] nerve (388.5)
- oculomotor [3rd, 4th, 6th] nerves (378.0-378.9)
- optic [2nd] nerve (377.0-377.9)
- peripheral autonomic nerves (337.0-337.9)
- neuralgia NOS or "rheumatic" (729.2)
- neuritis NOS or "rheumatic" (729.2)
- radiculitis NOS or "rheumatic" (729.2)
- peripheral neuritis in pregnancy (646.4)
- 350 Trigeminal nerve disorders
- Includes: disorders of 5th cranial nerve
- 350.1 Trigeminal neuralgia
- Tic douloureux
- Trifacial neuralgia
- Trigeminal neuralgia NOS
- Excludes: postherpetic (053.12)
- 350.2 Atypical face pain
- 350.8 Other specified trigeminal nerve disorders
- 350.9 Trigeminal nerve disorder, unspecified
- 351 Facial nerve disorders
- Includes: disorders of 7th cranial nerve
- Excludes: that in newborn (767.5)
- 351.0 Bell's palsy
- 351.1 Geniculate ganglionitis
- Geniculate ganglionitis NOS
- Excludes: herpetic (053.11)
- 351.8 Other facial nerve disorders
- Facial myokymia
- Melkersson's syndrome
- 351.9 Facial nerve disorder, unspecified
- 352 Disorders of other cranial nerves
- 352.0 Disorders of olfactory [1st] nerve
- 352.1 Glossopharyngeal neuralgia
- 352.2 Other disorders of glossopharyngeal [9th] nerve
- 352.3 Disorders of pneumogastric [10th] nerve
- Disorders of vagal nerve
- Excludes: paralysis of vocal cords or larynx (478.30-478.34)
- 352.4 Disorders of accessory [11th] nerve
- 352.5 Disorders of hypoglossal [12th] nerve
- 352.6 Multiple cranial nerve palsies
- Collet-Sicard syndrome
- Polyneuritis cranialis
- 352.9 Unspecified disorder of cranial nerves
- 353 Nerve root and plexus disorders
- Excludes: conditions due to:
- intervertebral disc disorders (722.0-722.9)
- spondylosis (720.0-721.9)
- vertebrogenic disorders (723.0-724.9)
- 353.0 Brachial plexus lesions
- Cervical rib syndrome
- Costoclavicular syndrome
- Scalenus anticus syndrome
- Thoracic outlet syndrome
- Excludes: brachial neuritis or radiculitis NOS (723.4)
- 353.1 Lumbosacral plexus lesions
- 353.2 Cervical root lesions, not elsewhere classified
- 353.3 Thoracic root lesions, not elsewhere classified
- 353.4 Lumbosacral root lesions, not elsewhere classified
- 353.5 Neuralgic amyotrophy
- Parsonage-Aldren-Turner syndrome
- 353.6 Phantom limb (syndrome)
- 353.8 Other nerve root and plexus disorders
- 353.9 Unspecified nerve root and plexus disorder
- 354 Mononeuritis of upper limb and mononeuritis multiplex
- 354.0 Carpal tunnel syndrome
- Median nerve entrapment
- Partial thenar atrophy
- 354.1 Other lesion of median nerve
- 354.2 Lesion of ulnar nerve
- Cubital tunnel syndrome
- Tardy ulnar nerve palsy
- 354.3 Lesion of radial nerve
- 354.4 Causalgia of upper limb
- Excludes: causalgia:
- NOS (355.9)
- lower limb (355.71)
- 354.5 Mononeuritis multiplex
- Combinations of single conditions classifiable to 354 or 355
- 354.8 Other mononeuritis of upper limb
- 354.9 Mononeuritis of upper limb, unspecified
- 355 Mononeuritis of lower limb
- 355.0 Lesion of sciatic nerve
- Excludes: sciatica NOS (724.3)
- 355.1 Meralgia paresthetica
- Lateral cutaneous femoral nerve of thigh compression or syndrome
- 355.2 Other lesion of femoral nerve
- 355.3 Lesion of lateral popliteal nerve
- Lesion of common peroneal nerve
- 355.4 Lesion of medial popliteal nerve
- 355.5 Tarsal tunnel syndrome
- 355.6 Lesion of plantar nerve
- Morton's metatarsalgia, neuralgia, or neuroma
- 355.7 Other mononeuritis of lower limb
- 355.71 Causalgia of lower limb
- Excludes: causalgia:
- NOS (355.9)
- upper limb (354.4)
- 355.79 Other mononeuritis of lower limb
- 355.8 Mononeuritis of lower limb, unspecified
- 355.9 Mononeuritis of unspecified site
- Causalgia NOS
- Excludes: causalgia:
- lower limb (355.71)
- upper limb (354.4)
- 356 Hereditary and idiopathic peripheral neuropathy
- 356.0 Hereditary peripheral neuropathy
- 356.1 Peroneal muscular atrophy
- Charcot-Marie-Tooth disease
- Neuropathic muscular atrophy
- 356.2 Hereditary sensory neuropathy
- 356.3 Refsum's disease
- Heredopathia atactica polyneuritiformis
- 356.4 Idiopathic progressive polyneuropathy
- 356.8 Other specified idiopathic peripheral neuropathy
- 356.9 Unspecified
- 357 Inflammatory and toxic neuropathy
- 357.0 Acute infective polyneuritis
- Guillain-Barre syndrome
- Postinfectious polyneuritis
- 357.1 Polyneuropathy in collagen vascular disease
- Code first underlying disease, as:
- disseminated lupus erythematosus (710.0)
- polyarteritis nodosa (446.0)
- rheumatoid arthritis (714.0)
- 357.2 Polyneuropathy in diabetes
- Code first underlying disease (250.6)
- 357.3 Polyneuropathy in malignant disease
- Code first underlying disease (140.0-208.9)
- 357.4 Polyneuropathy in other diseases classified elsewhere
- Code first underlying disease, as:
- amyloidosis (277.3)
- beriberi (265.0)
- deficiency of B vitamins (266.0-266.9)
- diphtheria (032.0-032.9)
- hypoglycemia (251.2)
- pellagra (265.2)
- porphyria (277.1)
- sarcoidosis (135)
- uremia (585)
- Excludes: polyneuropathy in:
- herpes zoster (053.13)
- mumps (072.72)
- 357.5 Alcoholic polyneuropathy
- 357.6 Polyneuropathy due to drugs
- Use additional E code to identify drug
- 357.7 Polyneuropathy due to other toxic agents
- Use additional E code to identify toxic agent
- 357.8 Other
- 357.9 Unspecified
- 358 Myoneural disorders
- 358.0 Myasthenia gravis
- 358.1 Myasthenic syndromes indiseases classified elsewhere
- Amyotrophy from stated cause classified elsewhere
- Eaton-Lambert syndrome from stated cause classified elsewhere
- Code first underlying disease, as:
- botulism (005.1)
- diabetes mellitus (250.6)
- hypothyroidism (244.0-244.9)
- malignant neoplasm (140.0-208.9)
- pernicious anemia (281.0)
- thyrotoxicosis (242.0-242.9)
- 358.2 Toxic myoneural disorders
- Use additional E code to identify toxic agent
- 358.8 Other specified myoneural disorders
- 358.9 Myoneural disorders, unspecified
- 359 Muscular dystrophies and other myopathies
- Excludes: idiopathic polymyositis (710.4)
- 359.0 Congenital hereditary muscular dystrophy
- Benign congenital myopathy
- Central core disease
- Centronuclear myopathy
- Myotubular myopathy
- Nemaline body disease
- Excludes: arthrogryposis multiplex congenita (754.89)
- 359.1 Hereditary progressive muscular dystrophy
- Muscular dystrophy:
- NOS
- distal
- Duchenne
- Erb's
- fascioscapulohumeral
- Gower's
- Landouzy-Déjérine
- limb-girdle
- ocular
- oculopharyngeal
- 359.2 Myotonic disorders
- Dystrophia myotonica
- Eulenburg's disease
- Myotonia congenita
- Paramyotonia congenita
- Steinert's disease
- Thomsen's disease
- 359.3 Familial periodic paralysis
- Hypokalemic familial periodic paralysis
- 359.4 Toxic myopathy
- Use additional E code to identify toxic agent
- 359.5 Myopathy in endocrinediseases classified elsewhere
- Code first underlying disease, as:
- Addison's disease (255.4)
- Cushing's syndrome (255.0)
- hypopituitarism (253.2)
- myxedema (244.0-244.9)
- thyrotoxicosis (242.0-242.9)
- 359.6 Symptomatic inflammatory myopathy in diseases classified elsewhere
- Code first underlying disease, as:
- amyloidosis (277.3)
- disseminated lupus erythematosus (710.0)
- malignant neoplasm (140.0-208.9)
- polyarteritis nodosa (446.0)
- rheumatoid arthritis (714.0)
- sarcoidosis (135)
- scleroderma (710.1)
- Sjögren's disease (710.2)
- 359.8 Other myopathies
- 359.9 Myopathy, unspecified