Disease #03263 (AT3D (antithrombin III deficiency (AT3D)), OMIM:613118)
Official abbreviation |
AT3D |
Name |
antithrombin III deficiency (AT3D) |
OMIM ID |
613118 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
SERPINC1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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