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1217370006: Laminin subunit alpha 5-related multisystemic syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Apr 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5036020015 LAMA5-related multisystemic syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
5036021016 Laminin subunit alpha 5-related multisystemic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
5036022011 Laminin subunit alpha 5-related multisystemic syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Laminin subunit alpha 5-related multisystemic syndrome Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Laminin subunit alpha 5-related multisystemic syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Laminin subunit alpha 5-related multisystemic syndrome Is a Systemic disease affecting skin true Inferred relationship Existential restriction modifier
Laminin subunit alpha 5-related multisystemic syndrome Is a Dermatosis of infancy true Inferred relationship Existential restriction modifier
Laminin subunit alpha 5-related multisystemic syndrome Is a Degenerative disorder of muscle true Inferred relationship Existential restriction modifier
Laminin subunit alpha 5-related multisystemic syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Laminin subunit alpha 5-related multisystemic syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Laminin subunit alpha 5-related multisystemic syndrome Is a Disorder of visual pathways true Inferred relationship Existential restriction modifier
Laminin subunit alpha 5-related multisystemic syndrome Is a Degeneration of retina true Inferred relationship Existential restriction modifier
Laminin subunit alpha 5-related multisystemic syndrome Occurrence Infancy true Inferred relationship Existential restriction modifier 3
Laminin subunit alpha 5-related multisystemic syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 3
Laminin subunit alpha 5-related multisystemic syndrome Finding site Structure of neuroepithelial layer of retina true Inferred relationship Existential restriction modifier 1
Laminin subunit alpha 5-related multisystemic syndrome Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Laminin subunit alpha 5-related multisystemic syndrome Finding site Skeletal and/or smooth muscle structure true Inferred relationship Existential restriction modifier 2
Laminin subunit alpha 5-related multisystemic syndrome Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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