Disease #00497 (F13BD (deficiency, factor XIII (B subunit) (F13BD)), OMIM:613235)
| Official abbreviation |
F13BD |
| Name |
deficiency, factor XIII (B subunit) (F13BD) |
| OMIM ID |
613235 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
120 |
| Phenotype entries for this disease |
120 |
| Associated with 1 gene |
F13B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-28 17:19:18 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|