icd 10 code for prader-willi syndrome

Is Prader Willi syndrome an eating disorder?

Prader-Willi Syndrome (PWS) PWS is the most common of the genetic disorders that cause life-threatening obesity in children. The syndrome affects many aspects of the person's life, including eating, behavior and mood, physical growth, and intellectual development. NICHD is one of many federal agencies and NIH Institutes working to understand PWS.

What is it like to live with Prader Willi syndrome?

Prader-Willi syndrome (PWS) is a genetic condition that affects many parts of the body. Infants with PWS have severe hypotonia (low muscle tone), feeding difficulties, and slow growth. In later infancy or early childhood, affected children typically begin to eat excessively and become obese.Other signs and symptoms often include short stature, hypogonadism, developmental delays, cognitive ...

What are the symptoms for Prade Willi syndrome?

These features may include:

• Food craving and weight gain. A classic sign of Prader-Willi syndrome is a constant craving for food, resulting in rapid weight gain, starting around age 2 years. ...
• Underdeveloped sex organs. ...
• Poor growth and physical development. ...
• Cognitive impairment. ...
• Delayed motor development. ...
• Speech problems. ...
• Behavioral problems. ...
• Sleep disorders. ...
• Other signs and symptoms. ...

What gene is affected in Prader Willi syndrome?

What are the symptoms of Prader-Willi syndrome (PWS)?

• Feeding and Metabolic Symptoms. An important early symptom of PWS is an infant's inability to suck, which affects the ability to feed.
• Physical Symptoms. ...
• Intellectual Symptoms. ...
• Behavioral and Psychiatric Symptoms. ...
• Stages of PWS Symptoms. ...

What is R68 89 diagnosis code?

ICD-10 code R68. 89 for Other general symptoms and signs is a medical classification as listed by WHO under the range - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified .

What is the ICD-10 code for global developmental delay?

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.

What is the ICD-10 code for cerebral palsy?

The ICD-10 Code for cerebral palsy is G80. 9.

What is the ICD-10 code for hypotonia?

P94. 2 - Congenital hypotonia | ICD-10-CM.

What is ICD-10 code F88?

ICD-10 code: F88 Other disorders of psychological development.

What is the ICD-10 code for neurodevelopmental disorder?

Mental, Behavioral and Neurodevelopmental disorders ICD-10-CM Code range F01-F99. The ICD-10 code range for Mental, Behavioral and Neurodevelopmental disorders F01-F99 is medical classification list by the World Health Organization (WHO).

What is the ICD-10 code for spastic cerebral palsy?

ICD-10 code G80. 1 for Spastic diplegic cerebral palsy is a medical classification as listed by WHO under the range - Diseases of the nervous system .

What is the ICD-10 code for autism?

The ICD-10-CM code for ASD—F84. 0 (autistic disorder)—should be the physician's or psychologist's diagnosis (typically required by payers) of the underlying medical condition, documented in the patient's medical record.

What is the ICD-10 code for Horner's syndrome?

ICD-10-CM Code for Horner's syndrome G90. 2.

What is R53 83?

ICD-9 Code Transition: 780.79 Code R53. 83 is the diagnosis code used for Other Fatigue. It is a condition marked by drowsiness and an unusual lack of energy and mental alertness. It can be caused by many things, including illness, injury, or drugs.

What is the ICD-10 code for Hypertonia?

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 .

What is the ICD-10 code for dystonia?

ICD-10 code G24. 9 for Dystonia, unspecified is a medical classification as listed by WHO under the range - Diseases of the nervous system .