Facial Cleft

Alias:
Craniofacial Cleft
Craniofacial Clefts
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Facial Cleft, also known as craniofacial cleft, is related to frontonasal dysplasia 1 and acromelic frontonasal dysostosis. An important gene associated with Facial Cleft is SMARCE1 (SWI/SNF Related, Matrix Associated, Actin Dependent Regulator Of Chromatin, Subfamily E, Member 1). The drugs Folic acid and Levoleucovorin have been mentioned in the context of this disorder. Affiliated tissues include bone and skin, and related phenotypes are nervous system and embryo
Related ID:
ICD11:11389088

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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6
35
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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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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
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References Literature

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