Congenital Anomalies of Kidney and Urinary Tract 1 (CAKUT1)

Alias:
Renal Hypodysplasia, Nonsyndromic, 1
Cakut1
Congenital Anomalies of the Kidney and Urinary Tract 1
Rhdns1
Kidney and Urinary Tract, Anomalies, Congenital, Susceptibility to, Type 1
Non-Syndromic Renal Hypodysplasia 1
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Anomalies of Kidney and Urinary Tract 1, also known as renal hypodysplasia, nonsyndromic, 1, is related to cakut and vacterl association, x-linked, with or without hydrocephalus. An important gene associated with Congenital Anomalies of Kidney and Urinary Tract 1 is DSTYK (Dual Serine/Threonine And Tyrosine Protein Kinase), and among its related pathways/superpathways is protein N-glycosylation processing phase (mammalian). The drugs Sulfamethoxazole and Cefixime have been mentioned in the context of this disorder. Affiliated tissues include kidney.
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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11
74
16

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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