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chromosome 18p deletion syndrome | RareConnect | RareConnect.io

/syndromic disease

/partial deletion of chromosome 18

/chromosome 18p deletion syndrome

chromosome 18p deletion syndrome

Rare Disease

MONDO:0007800

Also Known As

18p syndrome18p-De Grouchy syndromechromosome 18p deletionchromosome 18p deletion syndromedeletion 18p syndromemonosomy 18pmonosomy type 18ppartial deletion of chromosome 18ppartial deletion of the short arm of chromosome 18partial deletion of the short arm of chromosome type 18partial monosomy of chromosome 18ppartial monosomy of the short arm of chromosome 18

Definition

Monosomy 18p refers to a chromosomal disorder resulting from the deletion of all or part of the short arm of chromosome 18.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

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

External Resources

OMIM

OMIM:146390 ↗

Orphanet

Orphanet:1598 ↗Orphanet:261974 ↗

GARD

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