hemophilia C (Q1393718)
(Redirected from Q4135181)
human disease
- Congenital factor XI deficiency
- Hereditary factor XI deficiency disease (disorder)
- Rosenthal's disease
- plasma thromboplastin antecedent deficiency
- Hereditary factor XI deficiency disease
- haemophilia C
- Pta Deficiency
- Hereditary Factor XI Deficiency
- Rosenthal Syndrome
- Rosenthal factor deficiency
- FACTOR XI DEFICIENCY
- F11 Deficiency
- factor XI deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hemophilia C |
human disease |
|
Statements
1 reference
1 reference
1 reference
1 reference
5 references
286.2
2 references
1 reference
Identifiers
1 reference
1 reference
plasma thromboplastin antecedent
0 references
2 references
2 references
1 reference
Sitelinks
Wikipedia(8 entries)
- arwiki هيموفيليا ج
- bswiki Hemofilija C
- dewiki Faktor-XI-Mangel
- enwiki Haemophilia C
- eswiki Hemofilia C
- jawiki 第XI因子欠乏症
- ptwiki Hemofilia C
- ruwiki Гемофилия C