Iga nephropathy, susceptibility to, 3

Preferred Label : Iga nephropathy, susceptibility to, 3;

Symbol : IGAN3;

CISMeF acronym : IGAN3;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the sprouty RTK signaling antagonist 2 gene (SPRY2, 602466.0001);

Laboratory abnormalities : Proteinuria; Hematuria;

Prefixed ID : #616818;

Details

Origin ID

616818;

UMLS CUI

C4225194;

Genes related to phenotype
- Sprouty rtk signaling antagonist 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hematuria [HPO term]
- Hypertension [HPO term]
- IgA deposition in the glomerulus [HPO term]
- Mesangial hypercellularity [HPO term]
- Progressive [HPO term]
- Proteinuria [HPO term]
- Stage 5 chronic kidney disease [HPO term]
- Young adult onset [HPO term]
Semantic type(s)
- Finding [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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