Intellectual Developmental Disorder X Linked 110 C5774180
A genetic disorder affecting brain development, caused by mutations on the X chromosome. Primarily impacts males, with management through early intervention, therapies, and specialized educational approaches.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Seizures
Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Global developmental delay
(neurologic)Speech delay
(neurologic)Facial dysmorphism
(neurologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Applied Behavior Analysis (ABA) Therapy
Evidence-based behavioral intervention that uses positive reinforcement to improve social, communication, and learning skills through structured sessions tailored to individual needs.
Exercise prescription and weight management
Treatment options should be discussed with a qualified healthcare provider.
When to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Intellectual Developmental Disorder X Linked 110 C5774180?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Moeschler JB, Shevell M, Saul RA. Comprehensive evaluation of the child with intellectual disability or global developmental delays. Pediatrics. 2014.
van Bokhoven H, Schwartz K, Clayton DA. X-linked intellectual disability: phenotypic characterization and molecular analysis. Hum Genet. 2018.
Ropers HH, Hamel BC. X-linked mental retardation. Nat Rev Genet. 2005.
Kaufman L, Ayub M, Vincent JB. The genetic basis of non-syndromic intellectual disability: a review. J Neurodev Disord. 2010.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy