Genopathy
Gene-Disorder Association · Article
Gene
KLHL7
Kelch Like Family Member 7
Disorder
Fundus Dystrophy
First reported 2019
Supporting publications 13
Key publication · gene–disorder Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa.Orphanet journal of rare diseases · 2019
Key publication · disorder Further cases of a fundus dystrophy with unusual features.The British journal of ophthalmology · 1950
Manually curated
Association Review

In brief

The association between KLHL7 (Kelch Like Family Member 7) and Fundus Dystrophy is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording pathogenic variants.

Sources 2
Clinical variants 18
Symptoms 0
Compounds 0
Trials 0
Publications 13
01
At a glance

Association overview

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

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02
Provenance

Evidence and sources

2 sources

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

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03
KLHL7

The gene

1 source summary

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

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04
Fundus Dystrophy

The disorder

6 database identifiers

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

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05
ClinVar and variant evidence

Genetic basis

18 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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06
Literature

Reading

13 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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07
Provenance

References & sources

11 references

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

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