GALT
HGNC:4135 · SaudiVarKB evidence summary derived from retained literature mentions.
1Gene mentions
1Publications
0Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in GALT publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| intellectual disability | HP:0001249 | 1 | 1 |
| congenital cataract | — | 1 | 1 |
Linked variants
Variants normalized to GALT| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Saudi Arabia | — | — | 1 |
Supporting publications
1 records- 2022Co-Occurring Atypical Galactosemia and Wilson Disease.Molecular syndromologyPubMed ↗