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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 27-06-2023 |
Symbol | NDDOTSA |
Location | 6q16.1 |
Name | neurodevelopmental delay (NDD), obesity and autism spectrum disorder |
Corresponding gene | POU3F2 |
Main clinical features |
|
Genetic determination | not applicable |
Function/system disorder | psychiatry disorder |
Type | disease |
Remark(s) |