Intellectual Developmental Disorder Autosomal Recessive 70 C5193077
A genetic form of intellectual disability inherited when both parents carry the gene. It affects learning, communication, and daily living skills. Treatment involves comprehensive, lifelong supportive care.
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
Hypotonia
(neurologic)Speech delay
(neurologic)Global developmental 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
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Social Skills Training Group
Group-based intervention teaching interpersonal skills, emotional recognition, and appropriate social interactions in structured settings.
Additional treatment options
Gross Motor Development Program
Therapeutic exercises and activities designed to improve balance, coordination, strength, and overall motor functioning.
physical_therapyParent Education and Training
Structured parent training program covering behavior management techniques, communication strategies, and home-based intervention methods.
complementaryGrowth and Development Tracking
Regular monitoring of physical growth, developmental milestones, and associated medical conditions common in genetic disorders.
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 Recessive 70 C5193077?
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.
Kaufman L, Ayub M, Vincent JB. The genetic basis of non-syndromic intellectual disability: a review. J Neurodev Disord. 2020.
Moeschler JB, Shevell M, Saul RA, et al. Comprehensive evaluation of the child with intellectual disability or global developmental delays. Pediatrics. 2022.
Ropers HH, van der Zwaag B. Rare chromosomal deletions and duplications in intellectual disability: a clinical approach. Eur J Med Genet. 2021.
Chiurazzi P, Pizzo MT, Lisi E, Miranda MJ. Clinical genetics of autosomal recessive intellectual disability: bridging the gap between genotype and phenotype. Clin Genet. 2023.
Medication Comparisons
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View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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 27, 2026. · Read our editorial policy