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230561007: Congenital neuropathy with arthrogryposis multiplex congenita (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
345473013 Congenital neuropathy with arthrogryposis multiplex congenita en Synonym Active Entire term case insensitive SNOMED CT core module
618388015 Congenital neuropathy with arthrogryposis multiplex congenita (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
Congenital neuropathy with arthrogryposis multiplex congenita Is a Congenital polyneuropathy false Inferred relationship Existential restriction modifier
Congenital neuropathy with arthrogryposis multiplex congenita Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Finding site Nerve structure true Inferred relationship Existential restriction modifier 1
Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital neuropathy with arthrogryposis multiplex congenita Is a Neuropathy true Inferred relationship Existential restriction modifier
Congenital neuropathy with arthrogryposis multiplex congenita Is a Congenital anomaly of the peripheral nervous system false Inferred relationship Existential restriction modifier
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Congenital neuropathy with arthrogryposis multiplex congenita Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier 3
Congenital neuropathy with arthrogryposis multiplex congenita Is a Congenital anomaly of joint false Inferred relationship Existential restriction modifier
Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Contracture false Inferred relationship Existential restriction modifier 5
Congenital neuropathy with arthrogryposis multiplex congenita Finding site Joint structure false Inferred relationship Existential restriction modifier 5
Congenital neuropathy with arthrogryposis multiplex congenita Is a Arthrogryposis true Inferred relationship Existential restriction modifier
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Finding site Joint structure false Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Finding site Nerve structure false Inferred relationship Existential restriction modifier 4
Congenital neuropathy with arthrogryposis multiplex congenita Associated morphology Contracture true Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital neuropathy with arthrogryposis multiplex congenita Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital neuropathy with arthrogryposis multiplex congenita Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital neuropathy with arthrogryposis multiplex congenita Interprets Range of joint movement true Inferred relationship Existential restriction modifier 3
Congenital neuropathy with arthrogryposis multiplex congenita Has interpretation Decreased true Inferred relationship Existential restriction modifier 3
Congenital neuropathy with arthrogryposis multiplex congenita Finding site Structure of joint region 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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