Bowen-Conradi Syndrome (BWCNS)

Alias:
Bwcns
Bowen Syndrome, Hutterite Type
Bowen-Conradi Hutterite Syndrome
Bowen Hutterite Syndrome
Bowen Hutterite Syndrome, Formerly
Bowen Syndrome Hutterite Type
Fetal Growth Retardation
Hutterite Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Bowen-Conradi Syndrome, also known as bwcns, is related to cerebrooculofacioskeletal syndrome 1 and neural tube defects. An important gene associated with Bowen-Conradi Syndrome is EMG1 (EMG1 N1-Specific Pseudouridine Methyltransferase), and among its related pathways/superpathways are Processing of Capped Intron-Containing Pre-mRNA and rRNA processing in the nucleus and cytosol. The drugs Acetylsalicylic acid and Sodium citrate have been mentioned in the context of this disorder. Affiliated tissues include testes and brain, and related phenotypes are joint stiffness and microcephaly
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Antenatal
<1/1000000
21
87
9

Medical Symptom

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

Gene & Mutation

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Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
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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