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Repository for lectin-assisted multimodality data
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MIRAGE
congenital disorder of glycosylation type IIf
Summary
- Synonym
-
- CDG IIf
- CDG2F
- CDGIIf
- CMP-sialic acid transporter deficiency
- Carbohydrate deficient glycoprotein syndrome type IIf
- SLC35A1-CDG
- Definition
- A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the SLC35A1 gene on chromosome 6q15.
- Super Class
- autosomal recessive disease congenital disorder of glycosylation type II
External Links
- Disease Ontology
- DOID:0070258
- Mondo Disease Ontology
- MeSH
- UMLS
- ORDO
- GARD
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0011883 | Abnormal platelet granules |
| HP:0001875 | Neutropenia |
| HP:0002098 | Respiratory distress |
| HP:0001902 | Giant platelets |
| HP:0012418 | Hypoxemia |
| HP:0002090 | Pneumonia |
| HP:0003010 | Prolonged bleeding time |
| HP:0001933 | Subcutaneous hemorrhage |
| HP:0012143 | Abnormal megakaryocyte morphology |
| HP:0001892 | Abnormal bleeding |
