FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

763314009: Congenital muscular dystrophy with hyperlaxity (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3638515012 Congenital muscular dystrophy with hyperlaxity (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3638516013 Congenital muscular dystrophy with hyperlaxity en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital muscular dystrophy with hyperlaxity Is a Congenital muscular dystrophy false Inferred relationship Existential restriction modifier
Congenital muscular dystrophy with hyperlaxity Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital muscular dystrophy with hyperlaxity Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Congenital muscular dystrophy with hyperlaxity Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital muscular dystrophy with hyperlaxity Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with hyperlaxity Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with hyperlaxity Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with hyperlaxity Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with hyperlaxity Is a Congenital hereditary muscular dystrophy true Inferred relationship Existential restriction modifier
Congenital muscular dystrophy with hyperlaxity 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

Back to Start