(Q3331925)

English

myelomeningocele

spina bifida characterized by protrusion of the spinal cord through an opening, covered by meningeal membranes

Myelomeningocele
Meningomyelocele

In more languages

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

designated intractable/rare disease

1 reference

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

17 May 2019

class of disease

0 references

0 references

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

spinal cord disease

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

health specialty

medical genetics

0 references

anatomical location

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

external data available at URL

http://www.nanbyou.or.jp/entry/4633

language of work or name

1 reference

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

17 May 2019

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C101201

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

C98874

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

http://purl.obolibrary.org/obo/DOID_0060326

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0060326

1 reference

Identifiers.org

https://registry.identifiers.org/registry/doid

http://purl.obolibrary.org/obo/HP_0002475

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

http://www.orpha.net/ORDO/Orphanet_93969

0 references

Commons category

Spina bifida

0 references

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

C10.500.680.610

0 references

C16.131.666.680.610

0 references

Disease Ontology ID

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

Encyclopædia Britannica Online ID

science/meningomyelocele

subject named as

meningomyelocele

0 references

GARD rare disease ID

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Human Phenotype Ontology ID

2 references

Monarch Disease Ontology release 2018-06-29

28 July 2018

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

2 references

Disease Ontology

28 August 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

2 references

Disease Ontology

28 August 2019

Disease Ontology ID

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

0 references

Sitelinks

Wikipedia(2 entries)

fiwiki Meningomyeloseele
frwiki Myéloméningocèle

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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