Robinow-Sorauf Syndrome (RSS)

Alias:
Craniosynostosis-Bifid Hallux Syndrome
Acrocephalosyndactyly, Robinow-Sorauf Type
Acrocephalosyndactyly Robinow-Sorauf Type
Robinow Sorauf Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Robinow-Sorauf Syndrome, also known as craniosynostosis-bifid hallux syndrome, is related to saethre-chotzen syndrome and craniosynostosis 1. An important gene associated with Robinow-Sorauf Syndrome is TWIST1 (Twist Family BHLH Transcription Factor 1). Related phenotypes are downslanted palpebral fissures and hallux valgus
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
13
6

Medical Symptom

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

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

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
Journal
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IF
No Data Found!
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