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1156837002: 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

8 descendants. Search Descendants:

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

GB English

US English

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