P94.2 is a billable ICD code used to specify a diagnosis of congenital hypotonia. A 'billable code' is detailed enough to be used to specify a medical diagnosis. Hypotonia, also known as floppy baby syndrome, is a state of low muscle tone (the amount of tension or resistance to stretch in a muscle), often involving reduced muscle strength.
2016 2017 2018 2019 Billable/Specific Code Code on Newborn Record. P94.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/2019 edition of ICD-10-CM P94.2 became effective on October 1, 2018.
2018/19 ICD-10-CM Diagnosis Code E03.1. Congenital hypothyroidism without goiter. 2016 2017 2018 2019 Billable/Specific Code. E03.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
P94.2 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 P94.2 became effective on October 1, 2021. This is the American ICD-10-CM version of P94.2 - other international versions of ICD-10 P94.2 may differ.
ICD-10 Code for Congenital hypotonia- P94. 2- Codify by AAPC.
P94. 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 P94. 2 became effective on October 1, 2021.
ICD-10 code M62. 81 for Muscle weakness (generalized) is a medical classification as listed by WHO under the range - Soft tissue disorders .
ICD-10 code P94. 1 for Congenital hypertonia is a medical classification as listed by WHO under the range - Certain conditions originating in the perinatal period .
Medical Definition of hypotonia 1 : abnormally low pressure of the intraocular fluid. 2 : the state of having hypotonic muscle tone.
Congenital hypotonia is a medical term used to refer to poor muscle tone that's present at birth (congenital). It's not a disease but a sign of an underlying problem. Causes include central nervous system and muscle disorders. Sometimes, the cause can't be determined. Doctors call this benign congenital hypotonia.
Definition. Hypotonia is a medical term used to describe decreased muscle tone. Normally, even when relaxed, muscles have a very small amount of contraction that gives them a springy feel and provides some resistance to passive movement.
R53. 1 - Weakness. ICD-10-CM.
R53. 1 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 R53. 1 became effective on October 1, 2021.
60.
Hypertonia is too much muscle tone. Infants and newborns diagnosed with hypertonia have stiff muscles, especially their arms, legs and neck, which can be difficult to move. Muscle tone is the amount of resistance (tension) to movement in your muscles.
ICD-10 Code for Disorder of muscle, unspecified- M62. 9- Codify by AAPC.
Code is only used for patients less than 1 year old. P94.2 is a billable ICD code used to specify a diagnosis of congenital hypotonia.
Specialty: Pediatrics. MeSH Codes: D009123, D009123. ICD 9 Codes: 358 , 781.3.
This means that while there is no exact mapping between this ICD10 code P94.2 and a single ICD9 code, 779.89 is an approximate match for comparison and conversion purposes.
The ICD code P942 is used to code Hypotonia. Hypotonia, also known as floppy baby syndrome, is a state of low muscle tone (the amount of tension or resistance to stretch in a muscle), often involving reduced muscle strength.
Hypotonia is not a specific medical disorder, but a potential manifestation of many different diseases and disorders that affect motor nerve control by the brain or muscle strength. Recognizing hypotonia, even in early infancy, is usually relatively straightforward, but diagnosing the underlying cause can be difficult and often unsuccessful. ...
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This information is not intended for self-diagnosis and does not replace professional medical advice from a doctor.
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Hypothyroidism, congenital. Clinical Information. A condition in infancy or early childhood due to an in-utero deficiency of thyroid hormones that can be caused by genetic or environmental factors, such as thyroid dysgenesis or hypothyroidism in infants of mothers treated with thiouracil during pregnancy.
Clinical symptoms include severe mental retardation, impaired skeletal development, short stature, and myxedema. A deficiency of thyroid hormone present at birth. The etiology can be genetic or environmental, or a combination of both; treatment is based on severity and causality.
P94.2 is a valid billable ICD-10 diagnosis code for Congenital hypotonia . It is found in the 2021 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2020 - Sep 30, 2021 .
NEC Not elsewhere classifiable#N#This abbreviation in the Tabular List represents “other specified”. When a specific code is not available for a condition, the Tabular List includes an NEC entry under a code to identify the code as the “other specified” code.