icd 10 code for hereditary spastic paraplegia

Hereditary spastic paraplegia. G11.4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM G11.4 became effective on October 1, 2018.

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What is the ICD 10 code for spastic paraplegia?

Oct 01, 2021 · 2022 ICD-10-CM Diagnosis Code G11.4 Hereditary spastic paraplegia 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code G11.4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM G11.4 became effective on October 1, 2021.

What is hereditary spastic paraplegia?

Oct 01, 2021 · ICD-10-CM Code G11.4 Hereditary spastic paraplegia Billable Code G11.4 is a valid billable ICD-10 diagnosis code for Hereditary spastic paraplegia . It is found in the 2022 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2021 - Sep 30, 2022 .

What is spastic paraplegia type 4?

Hereditary spastic paraplegia BILLABLE | ICD-10 from 2011 - 2016 G11.4 is a billable ICD code used to specify a diagnosis of hereditary spastic paraplegia. A 'billable code' is detailed enough to be used to specify a medical diagnosis. The ICD code …

What is the ICD 10 code for cerebral palsy?

Hereditary spastic paraplegia (G11.4) G11.3 G11.4 G11.8 ICD-10-CM Code for Hereditary spastic paraplegia G11.4 ICD-10 code G11.4 for Hereditary spastic paraplegia is a medical classification as listed by WHO under the range - Diseases of the nervous system . Subscribe to Codify and get the code details in a flash.

What is hereditary spastic paraplegia?

Hereditary spastic paraplegia is a general term for a group of rare inherited disorders that cause weakness and stiffness in the leg muscles. Symptoms gradually get worse over time.

What is the ICD 10 code for functional paraplegia?

G82ICD-10 code G82 for Paraplegia (paraparesis) and quadriplegia (quadriparesis) is a medical classification as listed by WHO under the range - Diseases of the nervous system .

What is the ICD 10 code for spastic quadriplegia?

The spastic quadriparesis ICD 10 code is G82. 50 and can be used to indicate a diagnosis for reimbursement purposes.

Is Hereditary spastic paraplegia a form of MS?

The clinical similarities between Hereditary Spastic Paraplegia (HSP) and progressive MS, along with their analogous profiles of axonal loss in the long tracts, make the genes known to cause HSP biologically relevant candidates for the study of clinical outcome in MS.

What is a functional paraplegia?

Functional quadriplegia is the complete inability to move due to severe disability or frailty caused by another medical condition without physical injury or damage to the spinal cord(1).Sep 26, 2019

What is complete paraplegia?

Complete paraplegia occurs when the damage to the spinal cord is severe enough to completely cut off all connections between the brain and areas below the level of injury. Individuals with complete paraplegia will have no motor control or feeling below their level of injury.Nov 3, 2020

What is the ICD-10 code for muscle spasms?

ICD-10 | Muscle spasm (M62. 83)

What is the ICD-10 code for neuropathic pain?

2: Neuralgia and neuritis, unspecified.

What causes spastic cerebral palsy?

What Causes Spastic Cerebral Palsy? All types of cerebral palsy result from brain injury, damage, or malformation. Damage to the motor cortex in the brain causes spastic cerebral palsy. Most children develop cerebral palsy due to fetal development or brain damage that occurs during labor and delivery.Mar 17, 2022

Is spastic paraplegia dominant or recessive?

SPG13 HSP is an autosomal dominant form of uncomplicated HSP mapped to chromosome 2q24-34.

How is hereditary spastic paraplegia diagnosed?

The diagnosis of HSP is primarily by neurological examination and testing to rule ou... Hereditary spastic paraplegia (HSP), also called familial spastic paraparesis (FSP), refers to a group of inherited disorders that are characterized by progressive weakness and spasticity (stiffness) of the legs.Mar 27, 2019

Is spastic paraplegia a disability?

HSP refers to a group of inherited neurologic disorders that cause progressive weakness and spasticity, or stiffness, in the lower extremities, mostly the leg and hip muscles. The long-term prognosis for people diagnosed with HSP varies: Some become very disabled, while others experience only mild disability.

What is the approximate match between ICd9 and ICd10?

This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code G11.4 and a single ICD9 code, 334.1 is an approximate match for comparison and conversion purposes.

What is the ICD code for spastic paraplegia?

G11.4 is a billable ICD code used to specify a diagnosis of hereditary spastic paraplegia. A 'billable code' is detailed enough to be used to specify a medical diagnosis.

What is the name of the disease that causes stiffness and contraction in the lower limbs?

Hereditary spastic paraplegia (HSP), also known as hereditary spastic paraparesis, familial spastic paraplegias, French settlement disease, or Strumpell-Lorrain disease, is a group of inherited diseases whose main feature is progressive stiffness and contraction (spasticity) in the lower limbs, as a result of damage to or dysfunction of the nerves. ...

What is the genetic disorder of spastic paraplegia?

Spastic paraplegia type 8 Spastic paraplegia type 8 is part of a group of genetic disorders known as hereditary spastic paraplegias. These disorders are characterized by progressive muscle stiffness (spasticity) and the development of paralysis of the lower limbs (paraplegia).

What is a 5A?

Spastic paraplegia type 5A Spastic paraplegia type 5A is one of a group of genetic disorders known as hereditary spastic paraplegias. These disorders are characterized by muscle stiffness (spasticity) and severe weakness in the lower limbs (paraplegia).

How old is spastic paraplegia?

The signs and symptoms of spastic paraplegia type 3A usually appear before the age of 10; the average age of onset is 4 years. In some affected individuals the condition slowly worsens over time, sometimes leading to a need for walking support.

What is the name of the genetic disorder that causes paralysis of the lower limbs?

Troyer syndrome Troyer syndrome is part of a group of genetic disorders known as hereditary spastic paraplegias. These disorders are characterized by progressive muscle stiffness (spasticity) and the development of paralysis of the lower limbs (paraplegia).

What are the two types of spastic paraplegia?

Hereditary spastic paraplegias are divided into two types: pure and complex. Both types involve the lower limbs; the complex types may also involve the upper limbs, although to a lesser degree. In addition, the complex types may affect the brain and parts of the nervous system involved in muscle movement and sensations.

What are the characteristics of Troyer syndrome?

The most common characteristics of Troyer syndrome are spasticity of the leg muscles, progressive muscle weakness, paraplegia, muscle wasting in the hands and feet (distal amyotrophy), small stature, developmental delay, learning disorders, speech difficulties (dysarthria), and mood swings.

What does type 31 paraplegia feel like?

People with spastic paraplegia type 31 can also experience progressive muscle wasting (amyotrophy) in the lower limbs, exaggerated reflexes (hyperreflexia), a decreased ability to feel vibrations, reduced bladder control, and high-arched feet (pes cavus).

What causes paralysis of the lower limbs and trunk?

Complete paralysis of the lower half of the body including both legs, often caused by damage to the spinal cord. Paralysis of the legs and lower part of the body. Paralysis of the lower limbs and trunk. Severe or complete loss of motor function in the lower extremities and lower portions of the trunk.

What causes bilateral leg weakness?

This condition is most often associated with spinal cord diseases, although brain diseases; peripheral nervous system diseases; neuromuscular diseases; and muscular diseases may also cause bilateral leg weakness.

What is the G80?

congenital cerebral palsy ( G80.-) Complete or partial loss of movement in the lower part of the body, including both legs. Complete paralysis of the lower half of the body including both legs, often caused by damage to the spinal cord. Paralysis of the legs and lower part of the body.

What is paralysis of the legs?

Paraplegia with neurogenic bladder. Paraplegia, late effect of stroke. Clinical Information. Complete or partial loss of movement in the lower part of the body, including both legs.

What is the synonym for paraplegia?

Paraplegia (lower) NOS. Paraplegia. Approximate Synonyms. Paralytic syndrome of both lower limbs as sequela of stroke. Paraparesis. Paraparesis with paraplegia due to stroke. Paraplegia. Paraplegia (complete or partial paralysis of legs) Paraplegia (paralysis of legs) with neurogenic bladder.

What causes bilateral leg weakness?

This condition is most often associated with spinal cord diseases, although brain diseases; peripheral nervous system diseases; neuromuscular diseases; and muscular diseases may also cause bilateral leg weakness.

What causes paralysis of the lower leg?

Complete paralysis of the lower half of the body including both legs, often caused by damage to the spinal cord. Mild to moderate loss of bilateral lower extremity motor function, which may be a manifestation of spinal cord diseases; peripheral nervous system diseases; muscular diseases; intracranial hypertension; parasagittal brain lesions;

What is hysterical paralysis?

hysterical paralysis ( F44.4) Paraplegia (paraparesis) and quadriplegia (quadriparesis) Clinical Information. A slight paralysis or weakness of both legs. Complete or partial loss of movement in the lower part of the body, including both legs. Complete paralysis of the lower half of the body including both legs, ...