GINGF4 and Fibromatosis, Gingival, 4: Association Evidence

Gene-Disorder Association · Article

Gene

GINGF4

Gingival Fibromatosis, Hereditary, 4

Disorder

First reported 1986

Key publication · disorder Infantile systemic hyalinosis: report of four cases of a disease, fatal in infancy, apparently different from juvenile systemic hyalinosis.Pediatric pathology · 1986

Manually curated

Association Review

In brief

The association between GINGF4 (Gingival Fibromatosis, Hereditary, 4) and Fibromatosis, Gingival, 4 is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1

Clinical variants 0

Symptoms 0

Compounds 0

Trials 0

Publications 0

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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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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Fibromatosis, Gingival, 4

The disorder

5 database identifiers

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

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Provenance

References & sources

1 reference

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

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