APCDD1
HGNC:15718 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in APCDD1 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| inflammatory bowel disease | — | 1 | 1 |
| Crohn disease | — | 1 | 1 |
| congenital heart disease | — | 1 | 1 |
Linked variants
Variants normalized to APCDD1| 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 |
|---|
No structured population context is available.
Supporting publications
2 records- 2026A masked generative graph representation learning framework empowering precise spatial domain identification.Bioinformatics (Oxford, England)PubMed ↗
- 2023Predicting pediatric Crohn's disease based on six mRNA-constructed risk signature using comprehensive bioinformatic approaches.Open life sciencesPubMed ↗