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106152006: Second cranial nerve finding (finding)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
170579016 Second cranial nerve finding en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
578368015 Second cranial nerve finding (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2535643011 Optic nerve finding en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4892141000005115 fund vedr. 2. hjernenerve da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

9 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Second cranial nerve finding Is a Cranial nerve finding true Inferred relationship Some
Second cranial nerve finding Finding site Structure of nervous system (body structure) false Inferred relationship Some
Second cranial nerve finding Interprets Nervous system function false Inferred relationship Some
Second cranial nerve finding Is a Eye / vision finding false Inferred relationship Some
Second cranial nerve finding Finding site Optic nerve structure (body structure) true Inferred relationship Some 1
Second cranial nerve finding Is a Eye / vision finding true Inferred relationship Some
Second cranial nerve finding Is a Central nervous system finding true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Disorder of optic nerve Is a False Second cranial nerve finding Inferred relationship Some
Tumor invades optic nerve (finding) Is a False Second cranial nerve finding Inferred relationship Some
Optic disc finding Is a False Second cranial nerve finding Inferred relationship Some
Strachan's syndrome Is a False Second cranial nerve finding Inferred relationship Some
Toxic amblyopia Is a False Second cranial nerve finding Inferred relationship Some
Optic disc finding Is a False Second cranial nerve finding Inferred relationship Some
A rare neurodegenerative disorder belonging to the group of infantile progressive encephalopathies. Onset occurs during the first few weeks or months of life with hypotonia, poor feeding, drowsiness and abnormal movements. Infantile spasms, hypsarrhythmia and seizures appear during the first year of life. Visual loss, abnormal eye movements and optic atrophy also occur during infancy. Transmission appears to be autosomal recessive. A significant number of patients have been described who displayed most of the diagnostic criteria and features of PEHO syndrome, but did not appear to have cerebral atrophy on MRI, lacked the ophthalmologic signs and showed no reduction in CSF IGF-1 levels. This group of patients was diagnosed with PEHO-like syndrome. The prognosis is poor and most patients die before 15 years of age, mainly as a result of pneumonia or aspiration. Is a True Second cranial nerve finding Inferred relationship Some
A rare genetic autosomal recessive spastic ataxia disease with characteristics of the onset in early childhood of spastic paraparesis, cerebellar ataxia, dysarthria and optic atrophy. Caused by homozygous mutation in the MTPAP gene on chromosome 10p11. Is a True Second cranial nerve finding Inferred relationship Some
A rare, severe early-onset neurodegenerative encephalopathy characterized mainly by developmental delay (DD) / developmental regression (DR), epilepsy, cortical atrophy, secondary hypomyelination and thin corpus callosum. Additional features include secondary microcephaly, hypotonia, spasticity, optic atrophy and skeletal anomalies. Is a True Second cranial nerve finding Inferred relationship Some
A group of rare genetic neurodegenerative diseases with characteristics of infancy to childhood onset of progressive spastic paraplegia (with delayed motor milestones, gait disturbances, hyperreflexia and extensor plantar responses), optic atrophy (which may be accompanied by nystagmus and visual loss) and progressive peripheral neuropathy (with sensory impairment and distal muscle weakness/atrophy in upper and lower extremities). Additional signs may include foot deformities, spinal defects (scoliosis, kyphosis), joint contractures, exaggerated startle response, speech disorders, hyperhidrosis, extrapyramidal signs and intellectual disability. In very rare cases, a variant phenotype with less prominent or absent optic atrophy and/or neuropathy may be observed. Is a True Second cranial nerve finding Inferred relationship Some
A rare, X-linked leukodystrophy characterized primarily by spastic gait and autonomic dysfunction. When additional central nervous system (CNS) signs, such as intellectual deficit, ataxia, or extrapyramidal signs, are present, the syndrome is referred to as complicated SPG. Is a True Second cranial nerve finding Inferred relationship Some

This concept is not in any reference sets

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