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1208933000: 4H leukodystrophy (disorder)


Status: current, Primitive. Date: 31-Mar 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5013614018 4H leukodystrophy (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
5013615017 4H leucodystrophy en Synonym Active Initial character case insensitive SNOMED CT core
5013616016 4H leukodystrophy en Synonym Active Initial character case insensitive SNOMED CT core
5013617013 POLR-related leucodystrophy en Synonym Active Case sensitive SNOMED CT core
5013618015 POLR-related leukodystrophy en Synonym Active Case sensitive SNOMED CT core
5013619011 A rare hypomyelinating leucodystrophy disorder characterised by the association of dental abnormalities (delayed dentition, abnormal order of dentition, hypodontia), hypogonadotropic hypogonadism, and hypomyelinating leucodystrophy manifesting with neurodevelopmental delay or regression and/or progressive cerebellar symptoms. Age of onset typically ranges from infancy to childhood but exceptionally may occur in late adolescence or early adulthood. Mutations of the genes encoding POLR3 (RNA polymerase III) subunits, POLR3A, POLR3B and POLR1C, have been identified. The disease is inherited in an autosomal recessive manner. en Definition Active Case sensitive SNOMED CT core
5013620017 A rare hypomyelinating leukodystrophy disorder characterized by the association of dental abnormalities (delayed dentition, abnormal order of dentition, hypodontia), hypogonadotropic hypogonadism, and hypomyelinating leukodystrophy manifesting with neurodevelopmental delay or regression and/or progressive cerebellar symptoms. Age of onset typically ranges from infancy to childhood but exceptionally may occur in late adolescence or early adulthood. Mutations of the genes encoding POLR3 (RNA polymerase III) subunits, POLR3A, POLR3B and POLR1C, have been identified. The disease is inherited in an autosomal recessive manner. en Definition Active Case sensitive SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


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

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

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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