19.
Z72.810Child and adolescent antisocial behavior The 2022 edition of ICD-10-CM Z72. 810 became effective on October 1, 2021.
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 .
ICD-10 code: G93. 9 Disorder of brain, unspecified.
82 Altered mental status, unspecified.
Depression ICD-10 Codes F32. As stated above, F32. 9 describes major depressive disorder, single episode, unspecified.
Z71.2 as principal diagnosis According to the tabular index, a symbol next to the code indicates that it is an unacceptable principal diagnosis per Medicare code edits. This applies for outpatient and inpatient care.
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.
icd10 - Z712: Person consulting for explanation of examination or test findings.
I63. 9 - Cerebral infarction, unspecified | ICD-10-CM.
ICD-10-CM Code for Traumatic subdural hemorrhage without loss of consciousness S06. 5X0.
ICD-10-CM Code for Cerebral edema G93. 6.
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.
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.
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.
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.
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.
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.