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703535000: Mowat-Wilson syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
3008947016 Mowat-Wilson syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
3009119013 Mowat-Wilson syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
3009165011 Hirschsprung disease-mental retardation syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
3643142016 Hirschsprung disease-intellectual disability syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
3702281000052111 Mowat-Wilsons syndrom sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mowat-Wilson syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Mowat-Wilson syndrome (disorder) Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Mowat-Wilson syndrome (disorder) Is a Hirschsprung's disease true Inferred relationship Some
Mowat-Wilson syndrome (disorder) Is a Hereditary disorder of nervous system false Inferred relationship Some
Mowat-Wilson syndrome (disorder) Is a mental retardation false Inferred relationship Some
Mowat-Wilson syndrome (disorder) Finding site Parasympathetic nervous system structure false Inferred relationship Some
Mowat-Wilson syndrome (disorder) Finding site Autonomic nerve structure true Inferred relationship Some 3
Mowat-Wilson syndrome (disorder) Associated morphology kongenital dilatation false Inferred relationship Some 4
Mowat-Wilson syndrome (disorder) Associated morphology kongenital hypertrofi false Inferred relationship Some 4
Mowat-Wilson syndrome (disorder) Finding site Colon structure false Inferred relationship Some 4
Mowat-Wilson syndrome (disorder) Occurrence Congenital false Inferred relationship Some 5
Mowat-Wilson syndrome (disorder) Associated morphology Developmental anomaly (morphologic abnormality) false Inferred relationship Some 5
Mowat-Wilson syndrome (disorder) Finding site Structure of large intestine (body structure) false Inferred relationship Some 5
Mowat-Wilson syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Mowat-Wilson syndrome (disorder) Associated morphology kongenital dilatation false Inferred relationship Some 1
Mowat-Wilson syndrome (disorder) Finding site Colon structure false Inferred relationship Some 1
Mowat-Wilson syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Mowat-Wilson syndrome (disorder) Associated morphology kongenital hypertrofi false Inferred relationship Some 2
Mowat-Wilson syndrome (disorder) Finding site Colon structure false Inferred relationship Some 2
Mowat-Wilson syndrome (disorder) Is a Inherited autonomic nervous system disorder (disorder) true Inferred relationship Some
Mowat-Wilson syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Mowat-Wilson syndrome (disorder) Finding site Large intestine part false Inferred relationship Some 3
Mowat-Wilson syndrome (disorder) Occurrence Congenital false Inferred relationship Some 4
Mowat-Wilson syndrome (disorder) Finding site Large intestine part false Inferred relationship Some 4
Mowat-Wilson syndrome (disorder) Associated morphology kongenital hypertrofi false Inferred relationship Some 3
Mowat-Wilson syndrome (disorder) Is a Intellectual disability true Inferred relationship Some
Mowat-Wilson syndrome (disorder) Finding site Large intestine part true Inferred relationship Some 1
Mowat-Wilson syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Mowat-Wilson syndrome (disorder) Finding site Large intestine part true Inferred relationship Some 2
Mowat-Wilson syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Mowat-Wilson syndrome (disorder) Associated morphology Hypertrophy true Inferred relationship Some 2
Mowat-Wilson syndrome (disorder) Associated morphology Dilatation true Inferred relationship Some 1
Mowat-Wilson syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Mowat-Wilson syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Mowat-Wilson syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) Is a True Mowat-Wilson syndrome (disorder) Inferred relationship Some

This concept is not in any reference sets

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