(Q17146964)

English

neuronal migration disorder

human disease

Malformations of Cortical Development, Group II
cerebral malformation due to abnormal neuronal migration
Non-syndromic cerebral malformation due to abnormal neuronal migration
Brain malformation due to abnormal neuronal migration

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Statements

instance of

developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

malformation of cortical development

0 references

rare genetic developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0015572

cerebral malformation

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0015572

cerebral malformation with epilepsy

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Medical Subject Headings

NCI Thesaurus ID

C98990

0 references

exact match

http://purl.obolibrary.org/obo/HP_0002269

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0002269

http://www.orpha.net/ORDO/Orphanet_163209

0 references

topic's main category

Category:Neuronal migration disorders

0 references

Identifiers

MeSH descriptor ID

D054081

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

0 references

0 references

0 references

Human Phenotype Ontology ID

HP:0002269

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

LA05.5

Abnormal neuronal migration

0 references

Microsoft Academic ID

0 references

0 references

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

Orphanet ID

163209

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0002269

C5679571

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

Neuronal migration disorder

0 references

(Q17146964)

neuronal migration disorder

Statements

Identifiers

Sitelinks

Wikipedia(3 entries)

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