1156837002: Autosomal dominant distal hereditary motor neuropathy (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\...

\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant distal hereditary motor neuropathy (disorder)

\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant distal hereditary motor neuropathy (disorder)

\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant distal hereditary motor neuropathy (disorder)
\Disorder of body system\Disorder of nervous system (disorder)\Neuropathy (disorder)\Peripheral motor neuropathy\Autosomal dominant distal hereditary motor neuropathy (disorder)
\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Autosomal dominant distal hereditary motor neuropathy (disorder)
\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the peripheral nervous system\Peripheral motor neuropathy\Autosomal dominant distal hereditary motor neuropathy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4576298019 Autosomal dominant distal hereditary motor neuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4576299010 Autosomal dominant distal hereditary motor neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

10036081000172116 neuropathie motrice distale héréditaire autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

4241871000172112 autosomaal dominante distale motorische neuropathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal dominant distal hereditary motor neuropathy (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Autosomal dominant distal hereditary motor neuropathy (disorder)	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Some
Autosomal dominant distal hereditary motor neuropathy (disorder)	Finding site	Nerve structure	true	Inferred relationship	Some	1
Autosomal dominant distal hereditary motor neuropathy (disorder)	Finding site	Peripheral nervous system structure	true	Inferred relationship	Some	2
Autosomal dominant distal hereditary motor neuropathy (disorder)	Is a	Peripheral motor neuropathy	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Autosomal dominant spastic paraplegia type 17 (disorder)	Is a	True	Autosomal dominant distal hereditary motor neuropathy (disorder)	Inferred relationship	Some
Distal hereditary motor neuropathy type 1 (disorder)	Is a	True	Autosomal dominant distal hereditary motor neuropathy (disorder)	Inferred relationship	Some
Distal hereditary motor neuropathy type 7	Is a	True	Autosomal dominant distal hereditary motor neuropathy (disorder)	Inferred relationship	Some
Autosomal dominant congenital benign spinal muscular atrophy	Is a	True	Autosomal dominant distal hereditary motor neuropathy (disorder)	Inferred relationship	Some
Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome	Is a	True	Autosomal dominant distal hereditary motor neuropathy (disorder)	Inferred relationship	Some
Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome	Is a	True	Autosomal dominant distal hereditary motor neuropathy (disorder)	Inferred relationship	Some
Distal hereditary motor neuropathy type 5 (disorder)	Is a	True	Autosomal dominant distal hereditary motor neuropathy (disorder)	Inferred relationship	Some
Distal hereditary motor neuropathy type 2 (disorder)	Is a	True	Autosomal dominant distal hereditary motor neuropathy (disorder)	Inferred relationship	Some

Reference Sets