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719430008: Leber plus disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3316313012 Leber plus disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3316314018 Leber plus disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3316319011 Leber plus disease describes patients with the clinical features of Leber's hereditary optic neuropathy in combination with other serious systemic or neurological abnormalities. These abnormalities include: postural tremor, motor disorder, multiple sclerosis-like syndrome, spinal cord disease, skeletal changes, Parkinsonism with dystonia, anarthria, dystonia, motor and sensory peripheral neuropathy, spasticity and mild encephalopathy. It is caused by maternally inherited mitochondrial DNA (mtDNA) mutations. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
878301000172117 maladie de Leber plus fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
985031000172116 maladie de LHON plus fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
956061000172112 LHON (Leber hereditary optic neuropathy)-plus-ziekte nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
984251000172118 ziekte van Leber-plus nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leber plus disease (disorder) Is a Leber's optic atrophy true Inferred relationship Some
Leber plus disease (disorder) Associated morphology Primary atrophy true Inferred relationship Some 2
Leber plus disease (disorder) Occurrence Congenital true Inferred relationship Some 2
Leber plus disease (disorder) Finding site Optic nerve structure true Inferred relationship Some 2
Leber plus disease (disorder) Is a Congenital atrophy of optic nerve (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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