Genopathy
Gene-Disorder Association · Article
Gene
FYCO1
FYVE And Coiled-Coil Domain Autophagy Adaptor 1
Disorder
Cataract 44
First reported 1954
Supporting publications 1
Key publication · disorder [Brain abnormality with congenital cataract and hypotrichosis (Ullrich-Fremerey-Dohna); a contribution to constitutional typology and differential diagnosis].Zeitschrift fur Kinderheilkunde · 1954
Manually curated
Association Review

In brief

The association between FYCO1 (FYVE And Coiled-Coil Domain Autophagy Adaptor 1) and Cataract 44 is a manually-curated gene–disease association, drawing on a single expert-curated source, which records a causative germline mutation.

Sources 1
Clinical variants 0
Symptoms 4
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
FYCO1

The gene

1 source summary

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

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04
Cataract 44

The disorder

12 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

2 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

6 references

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

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