icd 10 code for gm2 gangliosidosis

What is the correct code assigned for a patient with Gangliosidosis gm3?

19.

What is diagnosis code Z71 2?

ICD-10 code Z71. 2 for Person consulting for explanation of examination or test findings is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .

What is code G93 9?

ICD-10 code: G93. 9 Disorder of brain, unspecified.

What is diagnosis code g7000?

Myasthenia gravis withoutMyasthenia gravis without (acute) exacerbation.

Is Z71 2 billable?

Z71. 2 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 Z71. 2 became effective on October 1, 2021.

What is I10 diagnosis?

ICD-Code I10 is a billable ICD-10 code used for healthcare diagnosis reimbursement of Essential (Primary) Hypertension.

What is the ICD-10 code for CVA?

I63. 9 - Cerebral infarction, unspecified | ICD-10-CM.

What is the ICD-10 code for subdural hematoma?

ICD-10-CM Code for Traumatic subdural hemorrhage without loss of consciousness S06. 5X0.

What is the ICD-10 code for right sided weakness?

Hemiplegia, unspecified affecting right dominant side The 2022 edition of ICD-10-CM G81. 91 became effective on October 1, 2021. This is the American ICD-10-CM version of G81.

What is the ICD-10 code for muscular dystrophy?

The ICD-10 Code for muscular dystrophy is G71. 0.

What is the ICD-10 code for myalgia?

ICD-10 code M79. 1 for Myalgia is a medical classification as listed by WHO under the range - Soft tissue disorders .

What is the ICD-10 code for dysphagia?

Code R13. 10 is the diagnosis code used for Dysphagia, Unspecified. It is a disorder characterized by difficulty in swallowing. It may be observed in patients with stroke, motor neuron disorders, cancer of the throat or mouth, head and neck injuries, Parkinson's disease, and multiple sclerosis.

Coding Notes for E75.09 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.

ICD-10-CM Alphabetical Index References for 'E75.09 - Other GM2 gangliosidosis'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E75.09. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

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 E75.09 and a single ICD9 code, 330.1 is an approximate match for comparison and conversion purposes.

ICD-10-CM Alphabetical Index References for 'E75.00 - GM2 gangliosidosis, unspecified'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E75.00. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

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 E75.00 and a single ICD9 code, 330.1 is an approximate match for comparison and conversion purposes.

What is the g-m1 ganglioside?

It is characterized by intralysosomal accumulation of g (m1) ganglioside and oligosaccharides, primarily in neurons of the central nervous system. The infantile form is characterized by muscle hypotonia, poor psychomotor development, hirsutism, hepatosplenomegaly, and facial abnormalities.

What is GC 3.2.1.23?

A ganglioside storage disorder due to beta-galactosidase (ec 3.2.1.23) deficiency and abnormal accumulation of gm1 ganglioside in neurons and in hepatic, splenic and other histiocytes and in renal glomerular epithelium due.

What is autosomal recessive lysosomal storage disease?

An autosomal recessive lysosomal storage disease characterized by deficiency of the enzyme acid beta-galactosidase, resulting in the accumulation of acid lipids in the nervous system. Signs and symptoms include neurologic disturbances, muscle atrophy, dystonia, eye abnormalities, and formation of angiokeratomas.