Other congenital malformations of musculoskeletal system. Q79.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2020 edition of ICD-10-CM Q79.8 became effective on October 1, 2019.
Congenital malformation syndromes predominantly affecting facial appearance. A syndrome of congenital facial paralysis, frequently associated with abducens palsy and other congenital abnormalities including lingual palsy, clubfeet, brachial disorders, cognitive deficits, and pectoral muscle defects.
An abnormality of the musculoskeletal system that is present at birth or detected in the neonatal period. Congenital structural abnormalities and deformities of the musculoskeletal system.
Q68.0 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 Q68.0 became effective on October 1, 2018. This is the American ICD-10-CM version of Q68.0 - other international versions of ICD-10 Q68.0 may differ.
5 for Muscle wasting and atrophy, not elsewhere classified is a medical classification as listed by WHO under the range - Soft tissue disorders .
ICD-10-CM Code for Disorder of muscle, unspecified M62. 9.
Disorder of muscle tone of newborn, unspecified P94. 9 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. 9 became effective on October 1, 2021.
ICD-10 code: P94. 2 Congenital hypotonia | gesund.bund.de.
ICD-10 code M62. 89 for Other specified disorders of muscle is a medical classification as listed by WHO under the range - Soft tissue disorders .
Disorder of muscle, unspecified M62. 9 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 M62. 9 became effective on October 1, 2021.
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.
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.
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-CM Code for Congenital hypertonia P94. 1.
315.9 - Unspecified delay in development | ICD-10-CM.
Encounter for screening for global developmental delays (milestones) Z13. 42 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Other congenital musculoskeletal deformities 1 Q68 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail. 2 The 2021 edition of ICD-10-CM Q68 became effective on October 1, 2020. 3 This is the American ICD-10-CM version of Q68 - other international versions of ICD-10 Q68 may differ.
The 2021 edition of ICD-10-CM Q68 became effective on October 1, 2020.
Congenital malformation characterized by micrognathia, glossoptosis and cleft palate.
A rare congenital malformation characterized by micrognathia, posterior retraction of the tongue, and cleft palate. A rare syndrome that is inherited in an autosomal dominant or recessive pattern and caused by mutations in the myh3 gene. It is a severe form of arthrogryposis.