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398040009: Charcot-Marie-Tooth disease, type I (disorder)


Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1765959019 Charcot-Marie-Tooth disease, type I (disorder) en Fully specified name Active Case sensitive SNOMED CT core
1777611019 Charcot-Marie-Tooth disease, type I en Synonym Active Case sensitive SNOMED CT core
1786062015 Hereditary sensory-motor neuropathy, type I en Synonym Active Initial character case insensitive SNOMED CT core
1786063013 Peroneal muscular atrophy of demyelinating type en Synonym Active Case insensitive SNOMED CT core
1786064019 Inherited dominant hypertrophic neuropathy en Synonym Active Case insensitive SNOMED CT core
1786065018 Hereditary motor and sensory neuropathy type I en Synonym Active Initial character case insensitive SNOMED CT core
1786066017 Charcot-Marie-Tooth disease of demyelinating type en Synonym Active Case sensitive SNOMED CT core
1786067014 HSMN, type I en Synonym Active Case sensitive SNOMED CT core
2966574017 Charcot Marie Tooth disease, type 1 en Synonym Active Case sensitive SNOMED CT core


7 descendants. Search Descendants:

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 Some
Charcot-Marie-Tooth disease, type I Finding site Peripheral nervous system structure true Inferred relationship Some 1
Charcot-Marie-Tooth disease, type I Associated morphology Neuropathic atrophy false Inferred relationship Some 1
Charcot-Marie-Tooth disease, type I Finding site Skeletal muscle structure false Inferred relationship Some 1
Charcot-Marie-Tooth disease, type I Finding site Skeletal muscle structure false Inferred relationship Some 1
Charcot-Marie-Tooth disease, type I Associated morphology Neuropathic atrophy false Inferred relationship Some 1
Charcot-Marie-Tooth disease, type I Is a Hereditary motor and sensory neuropathy true Inferred relationship Some
Charcot-Marie-Tooth disease, type I Is a Autosomal dominant hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
PMP2-related Charcot-Marie-Tooth disease type 1 Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Some
Charcot-Marie-Tooth disease, type IA Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Some
Charcot-Marie-Tooth disease, type IC Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Some
Charcot-Marie-Tooth disease, type IB Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Some
Charcot-Marie-Tooth disease type IE Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Some
Charcot-Marie-Tooth disease type 1D Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Some
Charcot-Marie-Tooth disease type 1F Is a True Charcot-Marie-Tooth disease, type I Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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