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719666002: 6q terminal deletion syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3317352014 6q terminal deletion syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3317353016 6q terminal deletion syndrome en Synonym Active Case insensitive SNOMED CT core
3317354010 Syndrome marked by a characteristic facial dysmorphism, short neck and psychomotor retardation, generally associated with a range of non-specific malformations. Isolated terminal 6q deletion syndrome is very rare with less than 20 cases being reported in the literature. The most frequent craniofacial anomalies include microcephaly, broad nose with prominent nasal root and bulbous nasal tip, large ears that may be malformed and low-set and a characteristic downturned mouth. The most commonly described neurological features are psychomotor retardation, hypotonia and seizures. Retinal anomalies are also common. The breakpoints are located between chromosome regions 6q25.3 and 6q26, within the fragile site FRA6E. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
6q terminal deletion syndrome Is a Anomaly of chromosome pair 6 false Inferred relationship Some
6q terminal deletion syndrome Is a Deletion of part of autosome false Inferred relationship Some
6q terminal deletion syndrome Occurrence Congenital true Inferred relationship Some 2
6q terminal deletion syndrome Finding site Chromosome pair 6 true Inferred relationship Some 2
6q terminal deletion syndrome Occurrence Congenital true Inferred relationship Some 3
6q terminal deletion syndrome Finding site Chromosome pair 6 true Inferred relationship Some 3
6q terminal deletion syndrome Associated morphology Deletion of long arm true Inferred relationship Some 2
6q terminal deletion syndrome Associated morphology Partial monosomy true Inferred relationship Some 3
6q terminal deletion syndrome Is a Deletion of part of long arm of chromosome 6 true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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