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1156840002: X-linked 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
4576305012 X-linked distal hereditary motor neuropathy en Synonym Active Entire term case sensitive SNOMED CT core module
4576306013 X-linked distal hereditary motor neuropathy (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked distal hereditary motor neuropathy Is a X-linked hereditary disease true Inferred relationship Existential restriction modifier
X-linked distal hereditary motor neuropathy Finding site Nerve structure true Inferred relationship Existential restriction modifier 2
X-linked distal hereditary motor neuropathy Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
X-linked distal hereditary motor neuropathy Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 1
X-linked distal hereditary motor neuropathy Is a Peripheral motor neuropathy true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Spinal muscular atrophy with respiratory distress type 2 Is a True X-linked distal hereditary motor neuropathy Inferred relationship Existential restriction modifier
X-linked distal spinal muscular atrophy type 3 Is a True X-linked distal hereditary motor neuropathy Inferred relationship Existential restriction modifier
X-linked distal arthrogryposis multiplex congenita Is a True X-linked distal hereditary motor neuropathy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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