Upshaw Schulman Syndrome (Q18604563)
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medical condition
- congenital thrombotic thrombocytopenic purpura
- Congenital ADAMTS13 Deficiency
- Microangiopathic Hemolytic Anemia, Congenital
- Upshaw Factor, Deficiency of
- Thrombotic Thrombocytopenic Purpura, Familial
- Upshaw-Schulman Syndrome
- THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP
- Thrombotic Microangiopathy, Familial
- THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL
- Microangiopathic Hemolytic Anemia
- Congenital TTP
- Familial TTP
- Congenital ADAMTS-13 deficiency
- TTP
- Schulman-Upshaw Syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Upshaw Schulman Syndrome |
medical condition |
|
Statements
4 references
287.33
1 reference
C131657
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(4 entries)
- arwiki متلازمة أبشاو شولمان
- azwiki Apşou-Şulman sindromu
- dewiki Upshaw-Schulman-Syndrom
- enwiki Upshaw–Schulman syndrome