Weill-Marchesani Syndrome 3 (WMS3)

Alias:
Wms3
Weill-Marchesani Syndrome 3, Recessive
Weill-Marchesani Syndrome, Type 3
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Weill-Marchesani Syndrome 3, is also known as wms3, and has symptoms including joint stiffness An important gene associated with Weill-Marchesani Syndrome 3 is LTBP2 (Latent Transforming Growth Factor Beta Binding Protein 2). Affiliated tissues include eye, and related phenotypes are short stature and joint stiffness
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
9
2

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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No data available

Disease Model

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Name
MGI
Related Gene
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Publications
No data available

References Literature

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IF
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