Genopathy
Gene-Disorder Association · Article
Gene
SLC29A3
Solute Carrier Family 29 Member 3
Disorder
Syndromic X-Linked Intellectual Disability Snyder Type
First reported 1969
Key publication · disorder Recessive sex-linked mental retardation in the absence of other recognizable abnormalities. Report of a family.Clinical pediatrics · 1969
Manually curated
Association Review

In brief

The association between SLC29A3 (Solute Carrier Family 29 Member 3) and Syndromic X-Linked Intellectual Disability Snyder Type is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 69
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.

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
SLC29A3

The gene

2 source summaries

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

Request access
04
Syndromic X-Linked Intellectual Disability Snyder Type

The disorder

7 database identifiers

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

Request access
05
Phenotype

Clinical features

66 clinical features

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

Request access
06
Mechanism overlap

Shared mechanisms

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

Request access
07
Provenance

References & sources

7 references

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

Request access