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
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