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890118006: Mowat-Wilson syndrome due to monosomy 2q22 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4009919017 Hirschsprung disease and intellectual disability due to del(2)(q22) en Synonym Active Entire term case sensitive SNOMED CT core module
4009920011 Hirschsprung disease and intellectual disability due to monosomy 2q22 en Synonym Active Entire term case sensitive SNOMED CT core module
4009921010 Mowat-Wilson syndrome due to monosomy 2q22 (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
4009922015 Hirschsprung disease and intellectual disability due to 2q22 microdeletion en Synonym Active Entire term case sensitive SNOMED CT core module
4009923013 Mowat-Wilson syndrome due to del(2)q(22) en Synonym Active Entire term case sensitive SNOMED CT core module
4009924019 Mowat-Wilson syndrome due to monosomy 2q22 en Synonym Active Entire term case sensitive SNOMED CT core module
4009925018 Mowat-Wilson syndrome due to 2q22 microdeletion en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mowat-Wilson syndrome due to monosomy 2q22 Is a Mowat-Wilson syndrome true Inferred relationship Existential restriction modifier
Mowat-Wilson syndrome due to monosomy 2q22 Associated morphology Dilatation true Inferred relationship Existential restriction modifier 3
Mowat-Wilson syndrome due to monosomy 2q22 Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Mowat-Wilson syndrome due to monosomy 2q22 Finding site Large intestine part true Inferred relationship Existential restriction modifier 3
Mowat-Wilson syndrome due to monosomy 2q22 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Mowat-Wilson syndrome due to monosomy 2q22 Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 4
Mowat-Wilson syndrome due to monosomy 2q22 Finding site Autonomic nerve structure true Inferred relationship Existential restriction modifier 4
Mowat-Wilson syndrome due to monosomy 2q22 Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Mowat-Wilson syndrome due to monosomy 2q22 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Mowat-Wilson syndrome due to monosomy 2q22 Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier 5
Mowat-Wilson syndrome due to monosomy 2q22 Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Mowat-Wilson syndrome due to monosomy 2q22 Finding site Large intestine part true Inferred relationship Existential restriction modifier 5
Mowat-Wilson syndrome due to monosomy 2q22 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 5
Mowat-Wilson syndrome due to monosomy 2q22 Due to Deletion of part of long arm of chromosome 2 true Inferred relationship Existential restriction modifier 1
Mowat-Wilson syndrome due to monosomy 2q22 Finding site Structure of peripheral part of autonomic nervous system true Inferred relationship Existential restriction modifier 2
Mowat-Wilson syndrome due to monosomy 2q22 Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Mowat-Wilson syndrome due to monosomy 2q22 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Mowat-Wilson syndrome due to monosomy 2q22 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Mowat-Wilson syndrome due to monosomy 2q22 Is a Gastrointestinal complication true Inferred relationship Existential restriction modifier
Mowat-Wilson syndrome due to monosomy 2q22 Interprets Intellectual ability true Inferred relationship Existential restriction modifier 6
Mowat-Wilson syndrome due to monosomy 2q22 Has interpretation Impaired true Inferred relationship Existential restriction modifier 6
Mowat-Wilson syndrome due to monosomy 2q22 Interprets Adaptation behavior true Inferred relationship Existential restriction modifier 7
Mowat-Wilson syndrome due to monosomy 2q22 Has interpretation Impaired true Inferred relationship Existential restriction modifier 7

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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