nervous system heredodegenerative disease (Q19001236)

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Human disease

• inherited neurodegenerative disorder
• Hereditary Neurodegenerative Disorder
• hereditary neurodegenerative disease
• genetic neurodegenerative disease
• Heredodegenerative Disorders, Nervous System

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Language	Label	Description	Also known as
English	nervous system heredodegenerative disease	Human disease	inherited neurodegenerative disorder Hereditary Neurodegenerative Disorder hereditary neurodegenerative disease genetic neurodegenerative disease Heredodegenerative Disorders, Nervous System

Statements

instance of

class of disease

0 references

subclass of

genetic disease

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0024237

neurodegeneration

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

3 July 2018

Mondo ID

MONDO_0015952

genetic nervous system disorder

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0015952

health specialty

neurology

1 reference

inferred from

Medical Subject Headings

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C97073

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

3 July 2018

Mondo ID

MONDO_0024237

exact match

http://purl.obolibrary.org/obo/DOID_894

1 reference

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:894

Identifiers

MeSH descriptor ID

D020271

mapping relation type

exact match

subject named as

Heredodegenerative Disorders, Nervous System

0 references

MeSH tree code

C16.320.400

0 references

C10.574.500

0 references

Disease Ontology ID

DOID:894

1 reference

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:894

KBpedia ID

NervousSystemHeredodegenerativeDisease

1 reference

stated in

KBpedia

retrieved

9 July 2020

Mondo ID

MONDO_0024237

0 references

Orphanet ID

183500

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

3 July 2018

Mondo ID

MONDO_0015952

UMLS CUI

C3273225

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

3 July 2018

Mondo ID

MONDO_0024237

C0751870

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

25 May 2023

C5680568

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

16 June 2023

 

Sitelinks

Wikipedia(0 entries)

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Wikibooks(0 entries)

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Wikinews(0 entries)

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Wikiquote(0 entries)

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Wikisource(0 entries)

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Wikiversity(0 entries)

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Wikivoyage(0 entries)

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Wiktionary(0 entries)

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Multilingual sites(0 entries)

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