667801000000102: Chromosomal anomalies NOS (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 01-Oct 2012. Module: SNOMED CT United Kingdom clinical extension module

Descriptions:

Id Description Lang Type Status Case? Module

1465531000000119 Chromosomal anomalies NOS (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module

1465541000000111 Chromosomal anomalies NOS en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Chromosomal anomalies NOS	Is a	Congenital disorder due to abnormality of chromosome number OR structure	false	Inferred relationship	Existential restriction modifier
Chromosomal anomalies NOS	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier
Chromosomal anomalies NOS	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Additional chromosome NOS	Is a	False	Chromosomal anomalies NOS	Inferred relationship	Existential restriction modifier
Deletion of chromosome NOS	Is a	False	Chromosomal anomalies NOS	Inferred relationship	Existential restriction modifier
Mosaicism NOS	Is a	False	Chromosomal anomalies NOS	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets