Disorders Of The Peripheral Nervous System ICD 9 Codes (350-359)


DISORDERS OF THE PERIPHERAL NERVOUS SYSTEM (ICD 9 CODES: 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
Facial 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)
that in newborn (767.6)
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
Code first any associated underlying disease, such as:
diabetes mellitus (249.6, 250.6)
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
Median nerve neuritis
354.2    Lesion of ulnar nerve
Cubital tunnel syndrome
Tardy ulnar nerve palsy
354.3    Lesion of radial nerve
Acute radial nerve palsy
354.4    Causalgia of upper limb
Complex regional pain syndrome type II of the upper limb
Excludes: causalgia:
NOS (355.9)
lower limb (355.71)
complex regional pain syndrome type II of the 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)
complex regional pain syndrome type II of the 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
Complex regional pain syndrome NOS
Excludes: causalgia:
lower limb (355.71)
upper limb (354.4)
complex regional pain syndrome:
lower limb (355.71)
upper limb (354.4)
356       Hereditary and idiopathic peripheral neuropathy
356.0    Hereditary peripheral neuropathy
Déjérine-Sottas disease
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
Supranuclear paralysis
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 (249.6, 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 (277.30-277.39)
beriberi (265.0)
chronic uremia (585.9)
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 NOS (586)
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
357.81  Chronic inflammatory demyelinating polyneuritis
357.82  Critical illness polyneuropathy
Acute motor neuropathy
357.89  Other inflammatory and toxic neuropathy
357.9    Unspecified
358       Myoneural disorders
358.0    Myasthenia gravis
358.00  Myasthenia gravis without (acute) exacerbation
358.01  Myasthenia gravis with (acute) exacerbation
Myasthenia gravis in crisis
358.1    Myasthenic syndromes in diseases classified elsewhere
Code first underlying disease, as:
botulism (005.1, 040.41-040.42)
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
358.3    Lambert-Eaton syndrome
Eaton-Lambert syndrome
358.30  Lambert-Eaton syndrome, unspecified
Lambert-Eaton syndrome NOS
358.31  Lambert-Eaton syndrome in neoplastic disease
Code first the underlying neoplastic disease
358.39  Lambert-Eaton syndrome in other diseases classified elsewhere
Code first the underlying conditions
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
Excludes: periodic paralysis (359.3)
359.21  Myotonic muscular dystrophy
Dystrophia myotonica
Myotonia atrophica
Myotonic dystrophy
Proximal myotonic myopathy (PROMM)
Steinert's disease
359.22  Myotonia congenita
Acetazolamide responsive myotonia congenita
Dominant form (Thomsen's disease)
Myotonia levior
Recessive form (Becker's disease)
359.23  Myotonic chondrodystrophy
Congenital myotonic chondrodystrophy
Schwartz-Jampel disease
359.24  Drug-induced myotonia
Use additional E code to identify drug
359.29  Other specified myotonic disorder
Myotonia fluctuans
Myotonia permanens
Paramyotonia congenita (of von Eulenburg)
359.3    Periodic paralysis
Familial periodic paralysis
Hyperkalemic periodic paralysis
Hypokalemic familial periodic paralysis
Hypokalemic periodic paralysis
Potassium sensitive periodic paralysis
Excludes: paramyotonia congenita (of von Eulenburg) (359.29)
359.4    Toxic myopathy
Use additional E code to identify toxic agent
359.5    Myopathy in endocrine diseases classified elsewhere
Code first underlying disease, as:
Addison's disease (255.41)
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 (277.30-277.39)
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)
359.7    Inflammatory and immune myopathies, NEC
359.71  Inclusion body myositis
IBM
359.79  Other inflammatory and immune myopathies, NEC
Inflammatory myopathy NOS
359.8    Other myopathies
359.81  Critical illness myopathy
Acute necrotizing myopathy
Acute quadriplegic myopathy
Intensive care (ICU) myopathy
Myopathy of critical illness
359.89  Other myopathies
359.9    Myopathy, unspecified

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