congenital hemolytic anemia
Information
- Disease name
- congenital hemolytic anemia
- Disease ID
- DOID:589
- Description
Disease area statistics
Chromosome band
| Gene symbol | Chromosome | Start | Stop | The number of variant |
|---|---|---|---|---|
| SPTA1 | 1 | 158,610,704 | 158,686,715 | 4 |
Annotation
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00061568 | Active, not recruiting | Phase 1/Phase 2 | Improving the Results of Bone Marrow Transplantation for Patients With Severe Congenital Anemias | July 16, 2004 | January 31, 2026 |
- Disase is a (Disease Ontology)
- DOID:583
- Cross Reference ID (Disease Ontology)
- GARD:6167
- Cross Reference ID (Disease Ontology)
- ICD10CM:D58.9
- Cross Reference ID (Disease Ontology)
- ICD9CM:282
- Cross Reference ID (Disease Ontology)
- MESH:D000745
- Cross Reference ID (Disease Ontology)
- NCI:C34379
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:42601008
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0002881
- Exact Synonym (Disease Ontology)
- congenital hemolytic anaemia
- Exact Synonym (Disease Ontology)
- hereditary hemolytic anaemia
- Exact Synonym (Disease Ontology)
- hereditary hemolytic anemia
- HPO alt_id (Human Phenotype Ontology)
- HP:0004811
- HPO alt_id (Human Phenotype Ontology)
- HP:0004824
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0004804