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699269005: Myofibrillar myopathy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2983495012 Myofibrillar myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
2983503012 Myofibrillar myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

11 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myofibrillar myopathy Is a Disorder of skeletal muscle true Inferred relationship Existential restriction modifier
Myofibrillar myopathy Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Muscular dystrophy Selcen type Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier
Muscle filaminopathy Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier
Spheroid body myopathy Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier
Distal myotilinopathy Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier
Late-onset distal myopathy Markesbery Griggs type Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier
Desmin-related myofibrillar myopathy Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier
Fatal infantile hypertonic myofibrillar myopathy Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier
Alpha-B crystallin-related late-onset myopathy Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier
Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier
Congenital generalized hypercontractile muscle stiffness syndrome Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier
Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome Is a True Myofibrillar myopathy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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