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787037000: Congenital muscular dystrophy type 1A (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3773565011 Merosin-negative congenital muscular dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module
3773566012 Congenital muscular dystrophy type 1A en Synonym Active Only initial character case insensitive SNOMED CT core module
3773567015 CMD1A - congenital muscular dystrophy type 1A en Synonym Active Entire term case sensitive SNOMED CT core module
3773568013 Congenital muscular dystrophy due to laminin alpha2 deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3773569017 Congenital muscular dystrophy type 1A (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3773570016 MCD1A - muscular congenital dystrophy type 1A en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital muscular dystrophy type 1A Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy type 1A Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Congenital muscular dystrophy type 1A Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy type 1A Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy type 1A Is a Congenital hereditary muscular dystrophy true Inferred relationship Existential restriction modifier
Congenital muscular dystrophy type 1A Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy type 1A Clinical course Progressive 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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