716456000: 3q29 microdeletion syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Developmental hereditary disorder\3q29 microdeletion syndrome
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\3q29 microdeletion syndrome
• \Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 3\Deletion of part of long arm of chromosome 3\3q29 microdeletion syndrome
• \Anomaly of chromosome pair 3\Deletion of part of chromosome 3\Deletion of part of long arm of chromosome 3\3q29 microdeletion syndrome
• \Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\3q29 microdeletion syndrome
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 3\Deletion of part of long arm of chromosome 3\3q29 microdeletion syndrome
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 3\Deletion of part of chromosome 3\Deletion of part of long arm of chromosome 3\3q29 microdeletion syndrome
• \Developmental disorder\Developmental hereditary disorder\3q29 microdeletion syndrome
• \Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\3q29 microdeletion syndrome

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3306036018	3q29 microdeletion syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3306037010	3q29 microdeletion syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3306038017	3q subtelomere deletion syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3306039013	Monosomy 3q29	en	Synonym	Active	Case insensitive	SNOMED CT core
3306040010	A recurrent subtelomeric deletion syndrome with variable clinical manifestations including intellectual deficit and dysmorphic features. It has been described in 23 patients. The clinical phenotype is extremely variable. The most common features include mild-to-moderate intellectual deficit and slightly dysmorphic facial features: microcephaly, long and narrow face, short philtrum, large posteriorly rotated ears and high nasal bridge. Autism and gait ataxia have been noted occasionally. The syndrome is caused by a recurrent deletion of the 3q subtelomeric region. Most of the deletions appear de novo but a few of them were inherited from mildly or non-affected parents.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start