307841000000108: Mowat - Wilson syndrome (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 01-Oct 2015. Module: SNOMED CT United Kingdom clinical extension module

Descriptions:

Id Description Lang Type Status Case? Module

551961000000119 Mowat - Wilson syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT United Kingdom clinical extension module

551971000000114 Mowat - Wilson syndrome en Synonym Active Entire term case sensitive SNOMED CT United Kingdom clinical extension module

557191000000119 Mowat-Wilson syndrome 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
Mowat - Wilson syndrome	Is a	Congenital disorder due to abnormality of chromosome number OR structure	false	Inferred relationship	Existential restriction modifier
Mowat - Wilson syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Mowat - Wilson syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Mowat - Wilson syndrome	Finding site	Chromosome structure	false	Inferred relationship	Existential restriction modifier	1
Mowat - Wilson syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier
Mowat - Wilson syndrome	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier	1
Mowat - Wilson syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	1
Mowat - Wilson syndrome	Finding site	Chromosome structure	false	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets