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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
infantile hypophosphatasia
Summary
- Synonym
-
- Hops
- phosphoethanolaminuria
- Definition
- A hypophosphatasia that has_material_basis_in homozygous or compound heterozygosity mutation in the gene encoding tissue-nonspecific alkaline phosphatase (ALPL) on chromosome 1p36.
- Super Class
- hypophosphatasia
External Links
- Disease Ontology
- DOID:0110914
- Mondo Disease Ontology
- ORDO
- OMIM
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | |
| P05187 | Alkaline phosphatase, placental type | |
| Q5VV63 | Attractin-like protein 1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001252 | Hypotonia |
| HP:0001363 | Craniosynostosis |
| HP:0001508 | Failure to thrive |
| HP:0001522 | Death in infancy |
| HP:0001561 | Polyhydramnios |
| HP:0001903 | Anemia |
| HP:0001945 | Fever |
| HP:0002013 | Vomiting |
| HP:0002019 | Constipation |
| HP:0002039 | Anorexia |
