About: myelomeningocele

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About: myelomeningocele Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

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

Attributes	Values
rdf:type	Item
description	sygdom (da) Krankheit (de) malattia (it) хвороба (uk) spina bifida characterized by protrusion of the spinal cord through an opening, covered by meningeal membranes (en) synnynnäinen selkäytimen epämuodostuma (fi)
exact match	wds:Q3331925-52DC3C54-9873-4EF8-9DAD-A85D0573252A wds:Q3331925-7364FD79-F430-4605-BFEE-4E890435E813 wds:Q3331925-B6A203DC-E68E-4921-A40E-792839CAFC36 wds:Q3331925-CED9D7F9-1945-4797-8413-A6BC2F95B936
exact match	http://purl.obolibrary.org/obo/DOID_0060326 http://purl.obolibrary.org/obo/HP_0002475 http://identifiers.org/doid/DOID:0060326 http://www.orpha.net/ORDO/Orphanet_93969
health specialty	wds:Q3331925-E7299D39-7B40-4A0C-89F3-1F84755DDF52
Mondo ID	wds:Q3331925-D3B15816-857D-420A-B596-8E001BF651C3
Disease Ontology ID	wds:Q3331925-F72A979D-FC3C-4A05-A77D-AA319303E39C
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0019773
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:0060326
health specialty	medical genetics
Mondo ID	MONDO_0019773
Disease Ontology ID	DOID:0060326
rdfs:label	rygmarvsbrok (da) Meningocele (es) Meningomyeloseele (fi) meningomyelocele (nl) myelomeningocele (en) myelomeningocele (nn) myéloméningocèle (fr)
skos:prefLabel	rygmarvsbrok (da) Meningocele (es) Meningomyeloseele (fi) meningomyelocele (nl) myelomeningocele (en) myelomeningocele (nn) myéloméningocèle (fr)
name	rygmarvsbrok (da) Meningocele (es) Meningomyeloseele (fi) meningomyelocele (nl) myelomeningocele (en) myelomeningocele (nn) myéloméningocèle (fr)
instance of	wds:Q3331925-0739D162-5C04-4A8F-AE78-1FBD5A86F365 wds:Q3331925-2A488678-4761-432A-B82D-6736B3F59F0E wds:Q3331925-88025C0F-85E8-4844-B0FA-966E156866E3
instance of	class of disease designated intractable/rare disease developmental defect during embryogenesis
subclass of	wds:Q3331925-0b10297e-4ec0-85e4-c901-c598d9632f1d wds:Q3331925-18CE7D1C-810F-406D-92FB-9A10E585D0EF wds:Q3331925-D5E87FAB-76F6-44AE-92EF-3EBE47DF8B5F
subclass of	spinal cord disease spina bifida meningocele
Encyclopædia Britannica Online ID	wds:Q3331925-EE6B3795-2F93-4140-8C60-7F2F02624FD9
Encyclopædia Britannica Online ID	science/meningomyelocele
Orphanet ID	wds:Q3331925-86687F86-6DE8-4944-8C59-03E720370B6A
ICD-10-CM	wds:Q3331925-01E6EB56-1011-43C8-9443-6B0CB576E420 wds:Q3331925-2204890D-359D-4259-97B2-69D346F00CDC wds:Q3331925-2A6A5FC2-1838-4610-B371-A9C1AC2FB301 wds:Q3331925-4D0A8B8A-726E-4C50-9B29-AA89F103D369 wds:Q3331925-4DBEBFE9-19E9-415E-AF32-68AFE848C7CC wds:Q3331925-55B9CC7B-E2B7-4312-B26B-4CE75F91B6A6 wds:Q3331925-81316AD7-8D76-4BC1-A7D1-40A598E59563 wds:Q3331925-A0B18BEB-EC45-4B90-AD0D-BDCD0591BEE7 wds:Q3331925-BB0C6790-0905-4576-844A-6404AB8EA271 wds:Q3331925-D185F98A-7958-42C2-A167-D68A4E2E0C91 wds:Q3331925-F76DA911-5DF0-42F4-999C-4332AC970570
GARD rare disease ID	wds:Q3331925-116AB73A-BEED-488B-96FF-99B44F343366
Orphanet ID	93969
ICD-10-CM	Q05 Q05.9 Q05.0 Q05.1 Q05.2 Q05.3 Q05.4 Q05.5 Q05.6 Q05.7 Q05.8
GARD rare disease ID	3475
anatomical location	wds:Q3331925-3404A20F-6733-497E-A069-E1ED562A7ED2
anatomical location	spinal cord
Human Phenotype Ontology ID	wds:Q3331925-0463B0D5-D5AF-45FB-B880-E3625FBF901B
Human Phenotype Ontology ID	HP:0002475
Commons category	wds:Q3331925-1855BCE8-F794-47BE-874F-A5ECA5B2A84F
Commons category	Spina bifida
skos:altLabel	MMC (nn) Meningomyelocele (en) Myelomeningocele (en) Meningomyeloceele (fi) Meningomyelocele (fi) Myelomeningocele (fi) Myelomeningocele (fr) Myelomeningoseele (fi) Selkäydinhalkio (fi) Selkäydinkohju (fi)

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