(Q5445904)

English

Fetal hydantoin syndrome

medical condition

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

In more languages

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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

28 July 2018

0 references

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

28 July 2018

0 references

759.89

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

C98927

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

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

28 July 2018

1 reference

imported from Wikimedia project

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

imported from Wikimedia project

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

LD2F.01

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

0 references

0 references

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

28 July 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016008

(Q5445904)

Fetal hydantoin syndrome

Statements

Identifiers

Sitelinks

Wikipedia(4 entries)

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)