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Nephrotic Syndrome, Type 19 (NPHS19)

Alias:
Nphs19
Nephrotic Syndrome Type 19
Nephrotic Syndrome 19
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Nephrotic Syndrome, Type 19, is also known as nphs19. An important gene associated with Nephrotic Syndrome, Type 19 is NUP160 (Nucleoporin 160). Affiliated tissues include kidney, and related phenotypes are proteinuria and focal segmental glomerulosclerosis
Related ID：
MALACARDS：NPH107
OMIM：618178
MESH：D009404

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
4
1
NPH107

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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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
No Data Found!
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