Disease #06215 (IGAN3 ({?IgA nephropathy, susceptibility to, 3}), OMIM:616818)

Official abbreviation IGAN3
Name {?IgA nephropathy, susceptibility to, 3}
OMIM ID 616818
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SPRY2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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