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


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

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) est un(e) (attribut) Mowat-Wilson syndrome (disorder) true Inferred relationship Some
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) morphologie associée (attribut) dilatation true Inferred relationship Some 3
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) survenue (attribut) congénital true Inferred relationship Some 3
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) localisation d'une constatation (attribut) Large intestine part true Inferred relationship Some 3
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 4
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) localisation d'une constatation (attribut) Autonomic nerve structure true Inferred relationship Some 4
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) survenue (attribut) congénital true Inferred relationship Some 4
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) morphologie associée (attribut) hypertrophie true Inferred relationship Some 5
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) survenue (attribut) congénital true Inferred relationship Some 5
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) localisation d'une constatation (attribut) Large intestine part true Inferred relationship Some 5
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) Due to Deletion of part of long arm of chromosome 2 (disorder) true Inferred relationship Some 1
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) localisation d'une constatation (attribut) Structure of peripheral part of autonomic nervous system (body structure) true Inferred relationship Some 2
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 2
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) est un(e) (attribut) Gastrointestinal complication true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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