Disease #00101 (AT3D (Antithrombin III deficiency), OMIM:613118)
Official abbreviation |
AT3D |
Name |
Antithrombin III deficiency |
OMIM ID |
613118 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SERPINC1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|