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1162864000: Familial porencephaly (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4591809015 Familial porencephaly (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4591810013 Familial porencephalic cyst en Synonym Active Entire term case insensitive SNOMED CT core module
4591811012 Familial porencephaly en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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