Genopathy
Gene-Disorder Association · Article
Gene
SLC2A2
Solute Carrier Family 2 Member 2
Disorder
Endocrine System Disease
First reported 2009
Key publication · disorder [Etiological analysis and individualized treatment of pharyngeal paraesthesia].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2009
Manually curated
Association Review

In brief

The association between SLC2A2 (Solute Carrier Family 2 Member 2) and Endocrine System Disease is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 3
Compounds 0
Trials 0
Publications 0
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
SLC2A2

The gene

1 source summary

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

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04
Endocrine System Disease

The disorder

7 database identifiers

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

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05
Provenance

References & sources

3 references

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

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