52647008: Charcot-Marie-Tooth disease, type I (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

87618018 Charcot-Marie-Tooth disease, type I en Synonym Active Entire term case sensitive SNOMED CT core module

87619014 Hereditary sensory-motor neuropathy, type I en Synonym Active Only initial character case insensitive SNOMED CT core module

87620015 Inherited dominant hypertrophic neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module

87621016 HSMN, type I en Synonym Active Entire term case sensitive SNOMED CT core module

198400014 Peroneal muscular atrophy of demyelinating type en Synonym Active Entire term case insensitive SNOMED CT core module

496390011 Hereditary motor and sensory neuropathy type I en Synonym Active Only initial character case insensitive SNOMED CT core module

496391010 Hereditary sensory and autonomic neuropathy, type I en Synonym Active Only initial character case insensitive SNOMED CT core module

496392015 Dominant hereditary sensory neuropathy, type I en Synonym Active Only initial character case insensitive SNOMED CT core module

496393013 Acrodystrophic neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module

496394019 Charcot-Marie-Tooth disease of demyelinating type en Synonym Active Entire term case sensitive SNOMED CT core module

790679010 Charcot-Marie-Tooth disease, type I (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Charcot-Marie-Tooth disease, type I	Is a	Charcot-Marie-Tooth disease	false	Inferred relationship	Existential restriction modifier
Charcot-Marie-Tooth disease, type I	Associated morphology	Atrophy	false	Inferred relationship	Existential restriction modifier	1
Charcot-Marie-Tooth disease, type I	Associated morphology	Neuropathic atrophy	false	Inferred relationship	Existential restriction modifier	1
Charcot-Marie-Tooth disease, type I	Finding site	Nerve structure	false	Inferred relationship	Existential restriction modifier
Charcot-Marie-Tooth disease, type I	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier
Charcot-Marie-Tooth disease, type I	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier	1
Charcot-Marie-Tooth disease, type I	Is a	Neuropathy	false	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Charcot-Marie-Tooth disease, type IA	Is a	False	Charcot-Marie-Tooth disease, type I	Inferred relationship	Existential restriction modifier
Charcot-Marie-Tooth disease, type IC	Is a	False	Charcot-Marie-Tooth disease, type I	Inferred relationship	Existential restriction modifier
Charcot-Marie-Tooth disease, type IB	Is a	False	Charcot-Marie-Tooth disease, type I	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets