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3900008: Mixed sensory-motor polyneuropathy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
8504012 Mixed sensory-motor polyneuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
775372017 Mixed sensory-motor polyneuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
928121000195113 polineuropatia mista sensitivo-motoria it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3387880014 polyneuropathie sensitivomotrice mixte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mixed sensory-motor polyneuropathy Is a Motor polyneuropathy true Inferred relationship Some
Mixed sensory-motor polyneuropathy Is a Sensory polyneuropathy true Inferred relationship Some
Mixed sensory-motor polyneuropathy Finding site Nerve structure false Inferred relationship Some
Mixed sensory-motor polyneuropathy Finding site Peripheral nervous system structure false Inferred relationship Some
Mixed sensory-motor polyneuropathy Finding site Peripheral nerve structure true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Mixed sensorimotor polyneuropathy due to diabetes mellitus (disorder) Is a True Mixed sensory-motor polyneuropathy Inferred relationship Some
46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome is a rare, genetic, developmental defect during embryogenesis disorder characterized by partial (unilateral testis, persistence of Müllerian duct structures) or complete (streak gonads only) gonadal dysgenesis, usually manifesting with primary amenorrhea in individuals with female phenotype but 46,XY karyotype, and sensorimotor dysmyelinating minifascicular polyneuropathy, which presents with numbness, weakness, exercise-induced muscle cramps, sensory disturbances and reduced/absent deep tendon reflexes. Germ cell tumors (seminoma, dysgerminoma, gonadoblastoma) may develop from the gonadal tissue. Is a True Mixed sensory-motor polyneuropathy Inferred relationship Some
A rare, genetic, autosomal recessive axonal hereditary motor and sensory neuropathy disease characterized by prenatal onset of a severe sensorimotor axonal polyneuropathy (reflected by reduced fetal movement and polyhydramnios), manifesting, at birth, with respiratory failure requiring mechanical ventilation, profound muscular hypotonia, rapidly progressing distal muscle weakness, and absent deep tendon reflexes, in the absence of contractures, leading to death before 8 months of age. Neuropathological findings show severe loss of large- and medium-sized myelinated fibers without signs of demyelination. Is a True Mixed sensory-motor polyneuropathy Inferred relationship Some
A rare genetic neurological disorder with characteristics of childhood to adolescence onset of progressive demyelination occurring in episodes, sensorimotor polyneuropathy, and hearing loss. Disease progression and severity is variable. In general, in an increasing and decreasing course, patients eventually develop respiratory insufficiency, loss of motor skills and ambulation, ataxia, and cognitive decline. Vision problems and skin rashes are commonly reported. Is a True Mixed sensory-motor polyneuropathy Inferred relationship Some

Reference Sets

US English

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