FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

725420009: Congenital muscular dystrophy Paradas type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3442512013 Congenital muscular dystrophy Paradas type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3442513015 Congenital muscular dystrophy Paradas type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3442514014 Congenital myopathy Paradas type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5403469018 A rare congenital muscular dystrophy characterized by early onset of hypotonia, delayed motor development, and variably progressive generalized muscle weakness. Predominant involvement of pelvic and neck flexor muscles has been reported, as well as early involvement of hamstrings and medial gastrocnemius visible on muscle MRI. Serum creatine kinase levels are markedly elevated (in some cases already from early childhood). Muscle biopsy shows absence of dysferlin. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403470017 A rare congenital muscular dystrophy characterised by early onset of hypotonia, delayed motor development, and variably progressive generalised muscle weakness. Predominant involvement of pelvic and neck flexor muscles has been reported, as well as early involvement of hamstrings and medial gastrocnemius visible on muscle MRI. Serum creatine kinase levels are markedly elevated (in some cases already from early childhood). Muscle biopsy shows absence of dysferlin. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital muscular dystrophy Paradas type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital muscular dystrophy Paradas type (disorder) Is a Congenital muscular dystrophy false Inferred relationship Some
Congenital muscular dystrophy Paradas type (disorder) Occurrence Congenital false Inferred relationship Some 2
Congenital muscular dystrophy Paradas type (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 2
Congenital muscular dystrophy Paradas type (disorder) Occurrence Congenital false Inferred relationship Some 3
Congenital muscular dystrophy Paradas type (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 3
Congenital muscular dystrophy Paradas type (disorder) Associated morphology Dystrophy false Inferred relationship Some 2
Congenital muscular dystrophy Paradas type (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 3
Congenital muscular dystrophy Paradas type (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital muscular dystrophy Paradas type (disorder) Finding site Skeletal muscle structure true Inferred relationship Some 1
Congenital muscular dystrophy Paradas type (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Congenital muscular dystrophy Paradas type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital muscular dystrophy Paradas type (disorder) Is a Congenital hereditary muscular dystrophy true Inferred relationship Some
Congenital muscular dystrophy Paradas type (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start