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240080003: Benign congenital hypotonia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
359683018 Benign congenital hypotonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
629174016 Benign congenital hypotonia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
359683018 Benign congenital hypotonia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
359683018 Benign congenital hypotonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
629174016 Benign congenital hypotonia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
629174016 Benign congenital hypotonia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
149601000172114 hypotonie congénitale bénigne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
149601000172114 hypotonie congénitale bénigne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Benign congenital hypotonia (disorder) Is a Congenital myopathy false Inferred relationship Existential restriction modifier (core metadata concept)
Benign congenital hypotonia (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Benign congenital hypotonia (disorder) Is a Congenital anomaly of skeletal muscle (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Benign congenital hypotonia (disorder) Finding site Skeletal muscle system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Benign congenital hypotonia (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Benign congenital hypotonia (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Benign congenital hypotonia (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Benign congenital hypotonia (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Benign congenital hypotonia (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Benign congenital hypotonia (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Benign congenital hypotonia (disorder) Is a Disorder of skeletal muscle true Inferred relationship Existential restriction modifier (core metadata concept)
Benign congenital hypotonia (disorder) Is a Congenital anomaly of muscle AND/OR tendon false Inferred relationship Existential restriction modifier (core metadata concept)
Benign congenital hypotonia (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Benign congenital hypotonia (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Benign congenital hypotonia (disorder) Finding site Skeletal muscle and/or tendon structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Benign congenital hypotonia (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Benign congenital hypotonia (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Benign congenital hypotonia (disorder) Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Benign congenital hypotonia (disorder) Is a Decreased muscle tone (finding) true Inferred relationship Existential restriction modifier (core metadata concept)
Benign congenital hypotonia (disorder) Interprets Muscle tone true Inferred relationship Existential restriction modifier (core metadata concept) 2
Benign congenital hypotonia (disorder) Has interpretation Decreased true Inferred relationship Existential restriction modifier (core metadata concept) 2
Benign congenital hypotonia (disorder) Is a Poor muscle tone true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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