Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
autoimmune lymphoproliferative syndrome type 4
Summary
- Synonym
-
- ALPS type 4
- ALPS type IV
- ALPS4
- RALD
- RAS-associated autoimmune leukoproliferative disease
- RAS-associated autoimmune leukoproliferative disorder
- autoimmune lymphoproliferative syndrome type IV
- Definition
- An autoimmune lymphoproliferative syndrome that has_material_basis_in somatic mutation in the NRAS gene or the KRAS gene on chromosome 12p12.
- Super Class
- autoimmune lymphoproliferative syndrome autosomal dominant disease
External Links
- Disease Ontology
- DOID:0110117
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001442 | Typified by somatic mosaicism |
| HP:0002719 | Recurrent infections |
| HP:0001875 | Neutropenia |
| HP:0005523 | Lymphoproliferative disorder |
| HP:0001973 | Autoimmune thrombocytopenia |
| HP:0012311 | Monocytosis |
| HP:0002240 | Hepatomegaly |
| HP:0001878 | Hemolytic anemia |
| HP:0002731 | Decreased lymphocyte apoptosis |
