Genopathy
Gene-Disorder Association · Article
Gene
SLC25A15
Solute Carrier Family 25 Member 15
Disorder
Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome
First reported 1988
Supporting publications 35
Key publication · gene–disorder Clinical, biochemical and ultrastructural study on the pathogenesis of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.Brain & development · 1988
Key publication · disorder Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.American journal of diseases of children (1960) · 1969
Manually curated
Association Review

In brief

The association between SLC25A15 (Solute Carrier Family 25 Member 15) and Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.

Sources 5
Clinical variants 415
Symptoms 73
Compounds 0
Trials 0
Publications 35
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

5 sources

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

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03
SLC25A15

The gene

1 source summary

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

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04
Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome

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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05
Phenotype

Clinical features

55 clinical features

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

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06
ClinVar and variant evidence

Genetic basis

415 clinical variants

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

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07
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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08
Literature

Reading

35 publications

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

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09
Provenance

References & sources

17 references

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

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