ORPHA:356947

3q26q27 microdeletion syndrome

Synonyms: Del(3)(q26q27) · Monosomy 3q26q27

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to 3q26q28 deletion syndrome

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	3q26q27 microdeletion syndrome	Del(3)(q26q27) · Monosomy 3q26q27
fr	Syndrome de microdélétion 3q26q27	Del(3)(q26q27) · Monosomie 3q26q27
de	Mikrodeletionssyndrom 3q26q27	Del(3)(q26q27) · Monosomie 3q26q27
es	Síndrome de microdeleción 3q26q27	Del(3)(q26q27) · Monosomía 3q26q27
it	Sindrome da microdelezione 3q26q27	Del(3)(q26q27) · Monosomia 3q26-q27 · Monosomia 3q26q27 · Sindrome da microdelezione 3q26-q27
nl	3q26q27-microdeletiesyndroom	Del(3)(q26q27) · Monosomie 3q26q27
pt	Síndrome de microdeleção 3q26q27
pl	Zespół mikrodelecji 3q26q27	Del(3)(q26q27) · Monosomia 3q26q27 · Monosomia 3q26-q27 · Zespół mikrodelecji 3q26-q27
cs	Mikrodeleční syndrom 3q26q27	Del(3)(q26q27) · Monozomie 3q26-q27 · Monozomie 3q26q27 · Mikrodeleční syndrom 3q26-q27
uk	Синдром мікроделеції 3q26q27	Del(3)(q26q27) · Моносомія 3q26q27
zh	3q26q27微缺失综合征	3q26q27单体
tr	3q26q27 mikrodelesyon sendromu	Del(3)(q26q27) · Monozomi 3q26q27

Definition in:

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	0018156	E		validated
UMLS	C4755255	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.