1187567002: Autosomal recessive intermediate Charcot-Marie-Tooth disease type D (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
• \Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Autosomal recessive intermediate Charcot-Marie-Tooth disease type D

Status: current, Primitive. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4674185017	Autosomal recessive intermediate Charcot-Marie-Tooth disease type D (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
4674186016	Autosomal recessive intermediate Charcot-Marie-Tooth disease type D	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
4674187013	A rare hereditary motor and sensory neuropathy with characteristics of childhood onset of unsteady gait, pes cavus, frequent falls and foot dorsiflexor weakness slowly progressing to distal upper and lower limb muscle weakness and atrophy, distal sensory impairment and reduced tendon reflexes. Additional symptoms may include bilateral sensorineural hearing impairment and neuropathic pain.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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