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1187120008: Stromme syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4669968019 Stromme syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4669969010 Apple peel intestinal atresia, ocular anomalies, microcephaly syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4669970011 Jejunal atresia, microcephaly, ocular anomalies syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4669971010 Stromme syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Stromme syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Stromme syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Stromme syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Stromme syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Stromme syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Stromme syndrome Pathological process Pathological developmental process 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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