60650002: Ring chromosome 9 syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital chromosomal disease\...
• \Ring chromosome\Ring chromosome 9 syndrome
• \Anomaly of chromosome pair\Anomaly of chromosome pair 9\Ring chromosome 9 syndrome
• \Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Ring chromosome 9 syndrome
• \Congenital disease\Congenital chromosomal disease\Ring chromosome\Ring chromosome 9 syndrome
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 9\Ring chromosome 9 syndrome
• \Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Ring chromosome 9 syndrome

Status: current, Defined. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
100762016	Ring chromosome 9 syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
799625013	Ring chromosome 9 syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4212337016	An autosomal anomaly with characteristics of variable clinical features, most commonly including developmental delay, some degree of intellectual disability, facial dysmorphism, microcephaly, congenital heart anomalies and variable genital, limb and skeletal anomalies.	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