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240080003: Benign congenital hypotonia (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
359683018 Benign congenital hypotonia en Synonym Active Entire term case insensitive SNOMED CT core module
629174016 Benign congenital hypotonia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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