Autism and Intellectual Disability Comprehensive Panel
Also known as: AID COMP
Use
The Autism and Intellectual Disability Comprehensive Panel is designed for comprehensive genetic evaluation of individuals with autism spectrum disorder (ASD) and/or intellectual disability (ID). The test includes a series of genetic assessments to identify potential genetic syndromes or metabolic disorders associated with these conditions. It aids clinicians in determining a genetic basis by evaluating patient's genomic variations and relevant biochemical markers linked to ASD and ID.
Special Instructions
This test requires informed consent for genetic testing, especially for New York patients, due to state regulations. Additionally, an Autism and Intellectual Disability Patient History Form must be submitted with the order. Clinical information including age, gender, diet, drug therapy, and family history is essential for accurate result interpretation; the Biochemical Genetics Patient History Form is available for download or by contacting ARUP Client Services.
Limitations
This test has not been cleared or approved by the US Food and Drug Administration, though it is performed in a CLIA-certified laboratory with established performance characteristics by ARUP Laboratories. Limitations include potential diagnostic errors due to rare sequence variations and possible undetectable rare FMR1 variants. Copy number variants below the platform resolution, sequence-level mutations, and low-level mosaicism may not be detected. Results may not provide specific structural information related to genomic imbalance, necessitating additional cytogenetic testing by chromosome analysis or FISH as warranted.
Methodology
Mass Spectrometry
Biomarkers
LOINC Codes
- 39001-3
- 30191-1
- 30551-6
- 51413-3
- 30531-8
- 30349-5
- 30358-6
- 30540-9
- 30541-7
- 30327-1
- 30328-9
- 30331-3
- 30332-1
- 30233-1
- 30565-6
- 30566-4
- 30564-9
- 30238-0
- 30190-3
- 30356-0
- 30357-8
- 30234-9
- 30235-6
- 30560-7
- 30542-5
- 30534-2
- 35656-8
- 30312-3
- 30237-2
- 45321-7
- 45322-5
- 41107-4
- 36913-2
- 20636-7
- 20637-5
- 20639-1
- 20640-9
- 20643-3
- 20642-5
- 20644-1
- 20645-8
- 20647-4
- 20648-2
- 20649-0
- 20650-8
- 20651-6
- 20652-4
- 14875-9
- 20655-7
- 20656-5
- 20657-3
- 20658-1
- 20660-7
- 20661-5
- 20646-6
- 22670-4
- 25112-4
- 25132-2
- 25136-3
- 29507-1
- 25101-7
- 25116-5
- 29509-7
- 29524-6
- 25083-7
- 25084-5
- 25085-2
- 25099-3
- 29859-6
- 25135-5
- 25134-8
- 25088-6
- 25089-4
- 29519-6
- 25137-1
- 46132-7
- 22672-0
- 33244-5
- 15045-8
- 14683-7
- 34155-2
- 34275-8
- 62375-1
- 11526-1
- 20634-2
- 26600-7
- 32227-1
- 26605-6
- 26604-9
- 26608-0
- 26609-8
- 26613-0
- 20659-9
- 26599-1
- 20638-3
- 26607-2
- 55876-7
- 26610-6
Result Turnaround Time
5-18 days
Related Documents
For more information, please review the documents below
Specimen
Urine
Volume
15 mL
Minimum Volume
10 mL
Container
ARUP Standard Tubes
Collection Instructions
Random urine collection. Avoid dilute urine when possible.
Patient Preparation
Morning void preferred.
Storage Instructions
Critical frozen; must be submitted separately when multiple tests are ordered.
Causes for Rejection
Specimens exposed to more than one freeze/thaw cycle. Specimens containing preservatives.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | Unacceptable |
| Refrigerated | Unacceptable |
| Frozen | 1 month |
