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764095005: Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3646023013 Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3646024019 Ataxia, delayed dentition, hypomyelination syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3646025018 Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a Congenital disease false Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a Leukodystrophy false Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a Cerebral atrophy true Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a Hereditary ataxia true Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 3
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Associated morphology Myelin sheath alteration true Inferred relationship Existential restriction modifier 2
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Associated morphology Atrophy true Inferred relationship Existential restriction modifier 1
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Finding site White matter structure of brain and spinal cord true Inferred relationship Existential restriction modifier 3
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Finding site Myelinated nerve fiber structure true Inferred relationship Existential restriction modifier 2
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a Hereditary degenerative disease of central nervous system false Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a 4H leukodystrophy true Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a Malformation of tooth true Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a Late tooth eruption true Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Finding site Gonadal endocrine structure true Inferred relationship Existential restriction modifier 5
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Finding site Structure of pars distalis of pituitary true Inferred relationship Existential restriction modifier 6
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Finding site Tooth structure true Inferred relationship Existential restriction modifier 4
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Associated morphology Maturation deceleration true Inferred relationship Existential restriction modifier 4
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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