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Chromosome 18P Deletion Syndrome (MONDO:0007800)

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

Overview

Category

Ontology ID

Internal:9144

Synonyms

18p syndrome

18p-

chromosome 18p deletion

chromosome 18p deletion syndrome

deletion 18p syndrome

monosomy type 18p

partial deletion of chromosome 18p

partial deletion of the short arm of chromosome 18

partial deletion of the short arm of chromosome type 18

partial monosomy of chromosome 18p

partial monosomy of the short arm of chromosome 18

Mapped terms

DOID:0060406

GARD:0020818

ICD9:758.39

MEDGEN:96604

MESH:C538309

NCIT:C84521

OMIM:146390

Orphanet:1598

Orphanet:261974

SCTID:270890001

UMLS:C0432442

icd11.foundation:121037615

Child terms

Unknown children.