chromosome 16p12.2-p11.2 deletion syndrome

Rare Disease

MONDO:0013320

Also Known As

16p11.2-p12.2 microdeletion syndrome16p11.2p12.2 microdeletion syndromeDel(16)(p11.2p12.2)chromosome 16p12.2-p11.2 deletion syndrome, isolated casesmonosomy 16p11.2-p12.2monosomy 16p11.2p12.2chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-MB

Definition

16p11.2-p12.2 microdeletion syndrome is a recently described syndrome characterized by developmental delay and facial dysmorphism.

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Comprehensive, easy-to-understand information about this condition

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Associated Genes

DEL16P12.1P11.2 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

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chromosome 16p12.2-p11.2 deletion syndrome

Also Known As

Definition

Patient-Friendly Information

Associated Genes

External Resources

OMIM

Orphanet

GARD

Related Diseases