Genopathy
Gene-Disorder Association · Article
Gene
WDFY1
WD Repeat And FYVE Domain Containing 1
Disorder
Rett Syndrome, Congenital Variant
First reported 1994
Supporting publications 1
Key publication · disorder Rett variants: a suggested model for inclusion criteria.Pediatric neurology · 1994
Association Review

In brief

The association between WDFY1 (WD Repeat And FYVE Domain Containing 1) and Rett Syndrome, Congenital Variant is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 0
Symptoms 133
Compounds 0
Trials 0
Publications 1
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

1 source

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

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03
WDFY1

The gene

1 source summary

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

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04
Rett Syndrome, Congenital Variant

The disorder

17 database identifiers

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

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05
Phenotype

Clinical features

107 clinical features

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

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06
Literature

Reading

1 publication

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

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07
Provenance

References & sources

8 references

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

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