Chromosome 17p13.3, Telomeric, Duplication Syndrome (SHFLD3)

Alias:
Split-Hand/foot Malformation with Long Bone Deficiency 3
Shfld3
Split-Hand/foot Malformation with Long Bone Deficiency, Type 3
Split-Hand-Foot Malformation with Long Bone Deficiency 3
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Chromosome 17p13.3, Telomeric, Duplication Syndrome, also known as split-hand/foot malformation with long bone deficiency 3, is related to split hand-foot malformation and split-hand/foot malformation with long bone deficiency 1. An important gene associated with Chromosome 17p13.3, Telomeric, Duplication Syndrome is SHFLD3 (Split-Hand/Foot Malformation With Long Bone Deficiency 3). Affiliated tissues include bone, and related phenotypes are split hand and brachydactyly
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Basic Information

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

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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References Literature

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