Chromosome 11p Deletion

Alias:
Chromosome 11p Deletion Syndrome
Chromosome 11, Deletion 11p
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Chromosome 11p Deletion, also known as chromosome 11, deletion 11p, is related to wilms tumor, aniridia, genitourinary anomalies, and impaired intellectual development syndrome and wilms tumor 5. An important gene associated with Chromosome 11p Deletion is LOC107982234 (WT1/WT1-AS Bi-Directional Promoter Region), and among its related pathways/superpathways are Mesodermal commitment pathway and Embryonic and Induced Pluripotent Stem Cells and Lineage-specific Markers. Affiliated tissues include testis and lung.
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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3
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Medical Symptom

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Description
HPO Frequency
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HPO Source Accession
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Gene & Mutation

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Related Drugs

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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