Fetal Hydantoin Syndrome

Alias:
Fetal Dihydantoin Syndrome
Phenytoin Embryofetopathy
Dysmorphism Due to Hydantoin
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Fetal Hydantoin Syndrome, also known as fetal dihydantoin syndrome, is related to phenytoin toxicity and neuroblastoma. An important gene associated with Fetal Hydantoin Syndrome is EPHX2 (Epoxide Hydrolase 2). Affiliated tissues include brain and skin, and related phenotypes are short nose and hearing abnormality
Related ID:
ICD11:1894344911

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Antenatal
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1
10
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Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
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Related Drugs

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Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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