SHFM5 and Split-Hand/Foot Malformation 5: Association Evidence

Gene-Disorder Association · Article

Gene

SHFM5

Split Hand/Foot Malformation (Ectrodactyly) Type 5

Disorder

First reported 1995

Key publication · disorder Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review.American journal of medical genetics · 1995

Manually curated

Association Review

In brief

The association between SHFM5 (Split Hand/Foot Malformation (Ectrodactyly) Type 5) and Split-Hand/Foot Malformation 5 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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Split-Hand/Foot Malformation 5

The disorder

10 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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