Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
hypotonia-cystinuria syndrome
Summary
- Synonym
-
- cystinuria with mitochondrial disease
- Definition
- A syndrome that has_material_basis_in homozygous deletion on chromosome 2p21 that disrupts the SLC3A1 and PREPL genes. The deletion ranges in size from 23.8 to 75.5 kb. Itis characterized_by neonatal and infantile hypotonia and failure to thrive, cystinuria type 1 and nephrolithiasis, growth retardation due to growth hormone deficiency, and minor facial dysmorphism.
- Super Class
- chromosomal deletion syndrome syndrome
External Links
- Disease Ontology
- DOID:0060858
- Mondo Disease Ontology
- MeSH
- ORDO
- OMIM
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q07837 | Amino acid transporter heavy chain SLC3A1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001510 | Growth delay |
| HP:0012378 | Fatigue |
| HP:0000787 | Nephrolithiasis |
| HP:0002007 | Frontal bossing |
| HP:0000286 | Epicanthus |
| HP:0001611 | Hypernasal speech |
| HP:0003128 | Lactic acidosis |
| HP:0001252 | Hypotonia |
| HP:0000268 | Dolichocephaly |
| HP:0001558 | Decreased fetal movement |
