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771267003: Congenital muscular dystrophy with integrin alpha-7 deficiency (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
3705354013 Congenital muscular dystrophy with integrin alpha-7 deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3705355014 Congenital muscular dystrophy with integrin alpha-7 deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3705356010 Congenital muscular dystrophy with ITGA7 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3705357018 Congenital muscular dystrophy with ITGA7 (integrin alpha-7) deficiency 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
Congenital muscular dystrophy with integrin alpha-7 deficiency Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with integrin alpha-7 deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Congenital muscular dystrophy with integrin alpha-7 deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with integrin alpha-7 deficiency Is a Congenital muscular dystrophy false Inferred relationship Existential restriction modifier
Congenital muscular dystrophy with integrin alpha-7 deficiency Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with integrin alpha-7 deficiency Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with integrin alpha-7 deficiency Is a Congenital hereditary muscular dystrophy true Inferred relationship Existential restriction modifier
Congenital muscular dystrophy with integrin alpha-7 deficiency 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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