Genopathy
Gene-Disorder Association · Article
Gene
SDCCAG8
SHH Signaling And Ciliogenesis Regulator SDCCAG8
Disorder
Nephronophthisis
First reported 1951
Key publication · disorder [Familial, juvenile nephronophthisis (idiopathic parenchymal contracted kidney)].Helvetica paediatrica acta · 1951
Manually curated
Association Review

In brief

The association between SDCCAG8 (SHH Signaling And Ciliogenesis Regulator SDCCAG8) and Nephronophthisis is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 6
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

Request access
03
SDCCAG8

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

Request access
04
Nephronophthisis

The disorder

12 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Phenotype

Clinical features

3 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
06
Mechanism overlap

Shared mechanisms

1 shared pathway

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

Request access
07
Provenance

References & sources

7 references

Every source and publication cited across this dossier, as one numbered reference list.

Request access