Definition

A chromosomal deletion syndrome that is characterized by intellectual disability, dysmorphic facies, psychiatric illness and autism spectrum disorder, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15.

[1]

Synonyms

15q11.2 microdeletion syndrome

Cross References

Parent Terms

Child Terms

None

Sources of Associations

Associated Genes

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Associated Alleles

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Associated Models

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chromosome 15q11.2 deletion syndrome

chromosome 15q11.2 deletion syndrome

Associated Genes

Associated Alleles

Associated Models