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1187465008: Autosomal dominant spastic paraplegia type 9A (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4673878014 Cataracts, motor neuropathy, short stature, skeletal anomalies syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4673879018 Autosomal dominant spastic paraplegia type 9A en Synonym Active Only initial character case insensitive SNOMED CT core module
4673882011 Autosomal dominant spastic paraplegia type 9A (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4674026017 Spastic paraparesis, amyotrophy, cataracts, gastroesophageal reflux syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4674027014 Spastic paraparesis, amyotrophy, cataracts, gastro-oesophageal reflux syndrome 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
Autosomal dominant spastic paraplegia type 9A Is a Complicated hereditary spastic paraplegia false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 9A Is a Autosomal dominant hereditary spastic paraplegia false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 9A Clinical course Progressive true Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 9A Finding site Lower limb structure false Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 9A Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 9A Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 9A Interprets Movement true Inferred relationship Existential restriction modifier 6
Autosomal dominant spastic paraplegia type 9A Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 4
Autosomal dominant spastic paraplegia type 9A Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 5
Autosomal dominant spastic paraplegia type 9A Interprets Movement observable true Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 9A Has interpretation Absent true Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 9A Is a Autosomal dominant complex hereditary spastic paraplegia 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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