86997002: Ring chromosome 10 syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital chromosomal disease\...
• \Ring chromosome\Ring chromosome 10 syndrome
• \Anomaly of chromosome pair\Anomaly of chromosome pair 10\Ring chromosome 10 syndrome
• \Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Ring chromosome 10 syndrome
• \Congenital disease\Congenital chromosomal disease\Ring chromosome\Ring chromosome 10 syndrome
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 10\Ring chromosome 10 syndrome
• \Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Ring chromosome 10 syndrome

Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
144281015	Ring chromosome 10 syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
829377015	Ring chromosome 10 syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4212336013	An autosomal anomaly with characteristics of variable clinical features, depending on the size and precise location of deleted chromosome segments. Most patients present with developmental delay, intellectual disability, growth retardation, microcephaly, clinodactyly and dysmorphic features. Congenital heart disease and genitourinary anomalies are reported in some cases.	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

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