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1162864000: Familial porencephaly (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4591809015 Familial porencephaly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4591810013 Familial porencephalic cyst en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4591811012 Familial porencephaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6158791000241111 porencéphalie familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3424481001000111 Porenzephalie, familiäre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial porencephaly (disorder) Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
Familial porencephaly (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Familial porencephaly (disorder) Is a Porencephalic cyst true Inferred relationship Some
Familial porencephaly (disorder) Finding site Cerebral hemisphere structure (body structure) true Inferred relationship Some 1
Familial porencephaly (disorder) Associated morphology Cyst true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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