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1208933000: 4H leukodystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5013614018 4H leukodystrophy (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
5013615017 4H leucodystrophy en Synonym Active Only initial character case insensitive SNOMED CT core module
5013616016 4H leukodystrophy en Synonym Active Only initial character case insensitive SNOMED CT core module
5013617013 POLR-related leucodystrophy en Synonym Active Entire term case sensitive SNOMED CT core module
5013618015 POLR-related leukodystrophy en Synonym Active Entire term case sensitive SNOMED CT core module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
4H leukodystrophy Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
4H leukodystrophy Is a Leukodystrophy true Inferred relationship Existential restriction modifier
4H leukodystrophy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
4H leukodystrophy Finding site Myelinated nerve fiber structure true Inferred relationship Existential restriction modifier 1
4H leukodystrophy Associated morphology Myelin sheath alteration true Inferred relationship Existential restriction modifier 1
4H leukodystrophy Finding site White matter structure of brain and spinal cord true Inferred relationship Existential restriction modifier 2
4H leukodystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 2
4H leukodystrophy Is a Hereditary disorder of tooth true Inferred relationship Existential restriction modifier
4H leukodystrophy Is a Hypogonadotropic hypogonadism true Inferred relationship Existential restriction modifier
4H leukodystrophy Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
4H leukodystrophy Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
4H leukodystrophy Is a Reproductive system hereditary disorder true Inferred relationship Existential restriction modifier
4H leukodystrophy Is a Disorder of tooth development true Inferred relationship Existential restriction modifier
4H leukodystrophy Finding site Structure of pars distalis of pituitary true Inferred relationship Existential restriction modifier 4
4H leukodystrophy Finding site Gonadal endocrine structure true Inferred relationship Existential restriction modifier 5
4H leukodystrophy Finding site Tooth structure true Inferred relationship Existential restriction modifier 3
4H leukodystrophy Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Odontoleukodystrophy Is a True 4H leukodystrophy Inferred relationship Existential restriction modifier
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Is a True 4H leukodystrophy Inferred relationship Existential restriction modifier
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome Is a True 4H leukodystrophy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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