(Q40103033)

28 July 2018

designated intractable/rare disease

1 reference

reference URL

https://ddrare.nibiohn.go.jp/

nervous system malformations

17 May 2019

class of disease

0 references

subclass of

0 references

neurodevelopmental disorder

0 references

megalencephaly

0 references

cerebral malformation

1 reference

28 July 2018

cerebral malformation with epilepsy

1 reference

28 July 2018

rare genetic developmental defect during embryogenesis

1 reference

external data available at URL

28 July 2018

0 references

0 references

http://www.nanbyou.or.jp/entry/4783

language of work or name

Japanese

1 reference

reference URL

https://ddrare.nibiohn.go.jp/

17 May 2019

ICD-9-CM

742.4

1 reference

28 July 2018

C177779

0 references

http://purl.obolibrary.org/obo/HP_0007206

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

http://www.orpha.net/ORDO/Orphanet_99802

HP:0007206

0 references

Identifiers

MeSH descriptor ID

D065705

subject named as

Hemimegalencephaly

1 reference

C16.131.666.507.400.249.500

28 July 2018

0 references

C10.500.507.400.249.500

0 references

C16.131.621.207.532.500

0 references

0 references

PatientsLikeMe condition ID

0 references

0 references

1 reference

28 July 2018

Google Knowledge Graph ID

/g/11dfvhqdz1

0 references

HP:0007206

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

0 references

1 reference

28 July 2018

Medical Dictionary for Regulatory Activities ID

10088459

1 reference

reference URL

https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

0 references

1 reference

26 January 2022

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

Orphanet ID

99802

1 reference

28 July 2018

1 reference

Human Phenotype Ontology release 2018-03-08

28 July 2018

1 reference

8 October 2018