Meckel Syndrome, Type 11 (MKS11)

Alias:
Meckel Syndrome 11
Mks11
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Meckel Syndrome, Type 11, also known as meckel syndrome 11, is related to joubert syndrome 20 and retinitis pigmentosa. An important gene associated with Meckel Syndrome, Type 11 is TMEM231 (Transmembrane Protein 231). Affiliated tissues include kidney and cerebellum, and related phenotypes are polycystic kidney dysplasia and oligohydramnios
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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
1
11

Medical Symptom

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Description
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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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