Genopathy
Gene-Disorder Association · Article
Gene
SLC35D1
Solute Carrier Family 35 Member D1
Disorder
Hypochondroplasia
First reported 1964
Key publication · disorder [HYPOCHONDROPLASIA].Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin · 1964
Manually curated
Association Review

In brief

The association between SLC35D1 (Solute Carrier Family 35 Member D1) and Hypochondroplasia is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 51
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
SLC35D1

The gene

1 source summary

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

Request access
04
Hypochondroplasia

The disorder

11 database identifiers

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

Request access
05
Phenotype

Clinical features

35 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

6 references

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

Request access