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770558006: Late-onset distal myopathy Markesbery Griggs type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3701261015 ZASP (Z-band alternatively spliced PDZ motif protein) related myofibrillar myopathy en Synonym Active Entire term case sensitive SNOMED CT core module
3701262010 Late-onset distal myopathy Markesbery Griggs type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3701263017 ZASP related myofibrillar myopathy en Synonym Active Entire term case sensitive SNOMED CT core module
3701264011 Late-onset distal myopathy Markesbery Griggs type en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Late-onset distal myopathy Markesbery Griggs type Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Late-onset distal myopathy Markesbery Griggs type Is a Myofibrillar myopathy true Inferred relationship Existential restriction modifier
Late-onset distal myopathy Markesbery Griggs type Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Late-onset distal myopathy Markesbery Griggs type Occurrence Adulthood true Inferred relationship Existential restriction modifier 1
Late-onset distal myopathy Markesbery Griggs type Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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