Congenital Anomalies of Kidney and Urinary Tract Syndrome with or Without Hearing Loss, Abnormal Ears, or Developmental Delay (CAKUTHED)

Alias:
Cakuthed
Anomalies, Congenital, Kidney and Urinary Tract Syndrome with/without Hearing Loss, Abnormal Ears, or Developmental Delay
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Anomalies of Kidney and Urinary Tract Syndrome with or Without Hearing Loss, Abnormal Ears, or Developmental Delay, also known as cakuthed, is related to cakut and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Congenital Anomalies of Kidney and Urinary Tract Syndrome with or Without Hearing Loss, Abnormal Ears, or Developmental Delay is PBX1 (PBX Homeobox 1), and among its related pathways/superpathways is Mesodermal commitment pathway. Affiliated tissues include kidney and heart, and related phenotypes are respiratory insufficiency and renal insufficiency
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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7
72
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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
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References Literature

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