Definition

A chromosomal deletion syndrome that has_material_basis_in a contiguous deletion of the 1q21.1 region on chromosome 1 and is characterized by an increases the risk of delayed development, intellectual disability, physical abnormalities, and neurological and psychiatric problems.

[1]

Synonyms

1q21.1 microdeletion syndrome
monosomy 1q21.1

Cross References

Parent Terms

chromosomal deletion syndrome

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 1q21.1 deletion syndrome

chromosome 1q21.1 deletion syndrome

Associated Genes

Associated Alleles

Associated Models