factor V deficiency
Information
- Disease name
- factor V deficiency
- Disease ID
- DOID:2216
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:1247
- Cross Reference ID (Disease Ontology)
- GARD:2237
- Cross Reference ID (Disease Ontology)
- ICD10CM:D68.2
- Cross Reference ID (Disease Ontology)
- MESH:D005166
- Cross Reference ID (Disease Ontology)
- MIM:227400
- Cross Reference ID (Disease Ontology)
- NCI:C98938
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:191284007
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0015499
- Exact Synonym (Disease Ontology)
- deficiency, labile
- Exact Synonym (Disease Ontology)
- Hereditary hypoproaccelerinaemia
- Exact Synonym (Disease Ontology)
- Labile factor deficiency
- Exact Synonym (Disease Ontology)
- Proaccelerin deficiency
- MeSH unique ID (MeSH (Medical Subject Headings))
- D005166