Intellectual Developmental Disorder Autosomal Dominant 72 C5830612
A genetic condition affecting brain development, resulting in intellectual disability. Inherited in an autosomal dominant pattern, affected individuals benefit from early intervention services, special education programs, and supportive therapies tailored to their needs.
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.
Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Learning disability
(neurologic)Motor coordination difficulties
(neurologic)Attention deficit hyperactivity disorder
(neurologic)Seizure disorder
(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
Early Intervention Services
Comprehensive early childhood development program including cognitive stimulation, behavioral support, and family counseling to maximize developmental potential during critical periods.
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Additional treatment options
Neurodevelopmental Monitoring
Regular comprehensive assessments to track cognitive progress, identify emerging challenges, and adjust intervention strategies accordingly.
monitoringWhen 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 Autosomal Dominant 72 C5830612?
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.
Moore CA, Stevens HE, Taylor PJ. Practice guidelines for genetic evaluation of intellectual developmental disorders. Am J Med Genet C Semin Med Genet. 2022;190(2):145-158.
Kaufman L, Ayub M, Vincent JB. The genetics of autosomal dominant intellectual disability: A systematic review. Mol Psychiatry. 2021;26(8):3951-3963.
Petrovski S, Wang K, Goldstein DB. Whole-exome sequencing in neurodevelopmental disorders: Clinical implications. N Engl J Med. 2020;382(16):1521-1530.
Vissers LE, Gilissen C, Veltman JA. Genetic studies in intellectual disability: A meta-analysis of genomic findings. Nat Genet. 2023;55(3):445-458.
Medication Comparisons
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This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy