Log In|Sign Up
ENNephrotic Syndrome, Type 7 (NPHS7)
Alias:
Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis
Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 7
Ig-Mediated Membranoproliferative Glomerulonephritis
Immunoglobulin-Mediated Mpgn
Nephrotic Syndrome Type 7
Ig-Mediated Mpgn
Nphs7
Nephrotic Syndrome, Type 7, with Membranoproliferative Glomerulonephritis
Nephrotic Syndrome Type 7 with Membranoptoliferative Glomerulonephritis
Nephrotic Syndrome Type 7 with Membranoproliferative Glomerulonephritis
Hemolytic Uremic Syndrome with Dgke Deficiency
Hemolytic Uremic Syndrome, Atypical 7
Hemolytic Uremic Syndrome Atypical 7
Hus with Dgke Deficiency
Nephrotic Syndrome 7
Ahus7
Favorite
Nephrotic Syndrome, Type 7, also known as immunoglobulin-mediated membranoproliferative glomerulonephritis, is related to membranoproliferative glomerulonephritis and c3 glomerulopathy. An important gene associated with Nephrotic Syndrome, Type 7 is DGKE (Diacylglycerol Kinase Epsilon), and among its related pathways/superpathways are Glycerophospholipid biosynthesis and Effects of PIP2 hydrolysis. Affiliated tissues include kidney and endothelial, and related phenotypes are thrombocytopenia and hemolytic anemia
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
