Fetal hydantoin syndrome (Q5445904)

From Wikidata

Jump to navigation Jump to search

medical condition

• fetal dilantin syndrome
• congenital hydantoin syndrome
• Dilantin Embryopathy
• Phenytoin Embryopathy
• Fetal dihydantoin syndrome
• Phenytoin embryofetopathy

edit

Language	Label	Description	Also known as
English	Fetal hydantoin syndrome	medical condition	fetal dilantin syndrome congenital hydantoin syndrome Dilantin Embryopathy Phenytoin Embryopathy Fetal dihydantoin syndrome Phenytoin embryofetopathy

Statements

instance of

head and neck disease

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

class of disease

0 references

subclass of

pregnancy category

0 references

teratogenic Pierre robin syndrome

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

fetal anticonvulsant syndrome

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

health specialty

medical genetics

0 references

ICD-9-CM

759.89

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

NCI Thesaurus ID

C98927

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

exact match

http://www.orpha.net/ORDO/Orphanet_1912

0 references

Identifiers

MeSH descriptor ID

C537922

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

DiseasesDB

33179

1 reference

imported from Wikimedia project

English Wikipedia

GARD rare disease ID

6435

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

ICD-10 ID

Q86.1

1 reference

imported from Wikimedia project

English Wikipedia

ICD-10-CM

Q86.1

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

ICD-11 ID (Foundation)

1894344911

0 references

ICD-11 ID (MMS)

LD2F.01

subject named as

Fetal hydantoin syndrome

0 references

ICD-9 ID

760.77

1 reference

imported from Wikimedia project

English Wikipedia

Medical Dictionary for Regulatory Activities ID

10016508

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

Microsoft Academic ID

2780995915

0 references

Mondo ID

MONDO_0016008

0 references

OMIM ID

132810

1 reference

imported from Wikimedia project

English Wikipedia

Orphanet ID

1912

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

UMLS CUI

C0265372

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

 

Sitelinks

Wikipedia(4 entries)

edit

• arwiki متلازمة هيدانتوين الجنينية
• dewiki Dihydantoin-Embryopathie
• enwiki Fetal hydantoin syndrome
• plwiki Płodowy zespół hydantoinowy

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q5445904&oldid=2087141441"