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1156837002: Autosomal dominant distal hereditary motor neuropathy (disorder)

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

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 SNOMED CT core module
4576299010 Autosomal dominant distal hereditary motor neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module

8 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant distal hereditary motor neuropathy Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant distal hereditary motor neuropathy Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Autosomal dominant distal hereditary motor neuropathy Finding site Nerve structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant distal hereditary motor neuropathy Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 2
Autosomal dominant distal hereditary motor neuropathy Is a Peripheral motor neuropathy true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant spastic paraplegia type 17 Is a True Autosomal dominant distal hereditary motor neuropathy Inferred relationship Existential restriction modifier
Distal hereditary motor neuropathy type 1 Is a True Autosomal dominant distal hereditary motor neuropathy Inferred relationship Existential restriction modifier
Distal hereditary motor neuropathy type 7 Is a True Autosomal dominant distal hereditary motor neuropathy Inferred relationship Existential restriction modifier
Autosomal dominant congenital benign spinal muscular atrophy Is a True Autosomal dominant distal hereditary motor neuropathy Inferred relationship Existential restriction modifier
Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome Is a True Autosomal dominant distal hereditary motor neuropathy Inferred relationship Existential restriction modifier
Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome Is a True Autosomal dominant distal hereditary motor neuropathy Inferred relationship Existential restriction modifier
Distal hereditary motor neuropathy type 5 Is a True Autosomal dominant distal hereditary motor neuropathy Inferred relationship Existential restriction modifier
Distal hereditary motor neuropathy type 2 Is a True Autosomal dominant distal hereditary motor neuropathy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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