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726609005: Autosomal recessive spastic paraplegia type 64 (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3450946018 Autosomal recessive spastic paraplegia type 64 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3450947010 Autosomal recessive spastic paraplegia type 64 en Synonym Active Case insensitive SNOMED CT core
3450948017 An extremely rare and complex form of hereditary spastic paraplegia reported in only 4 patients from 2 families to date. The disease has characteristics of spastic paraplegia (presenting between the ages of 1 to 4 years with abnormal gait) associated with microcephaly, amyotrophy, cerebellar signs (e.g. dysarthria) aggressiveness, delayed puberty and mild to moderate intellectual disability. SPG64 is due to mutations in the ENTPD1 gene (10q24.1), encoding ectonucleoside triphosphate diphosphohydrolase 1. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive spastic paraplegia type 64 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 64 Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 64 Clinical course Progressive true Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 64 Interprets Movement true Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 64 Finding site Structure of right lower limb true Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 64 Finding site Structure of left lower limb true Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 64 Interprets Movement observable true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 64 Has interpretation Absent true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 64 Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Autosomal recessive spastic paraplegia type 64 Is a Complicated hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 64 Occurrence Congenital false Inferred relationship Some
Autosomal recessive spastic paraplegia type 64 Finding site Structure of lower limb false Inferred relationship Some
Autosomal recessive spastic paraplegia type 64 Associated morphology Degeneration false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 64 Finding site Spinal cord structure false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 64 Finding site Cerebellar structure false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 64 Associated morphology Degeneration false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 64 Occurrence Congenital false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 64 Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 64 Occurrence Congenital false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 64 Finding site Structure of lower limb false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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