congenital high-molecular-weight kininogen deficiency
MeSH: C537060ORPHA: 483
Overview
rare autosomal recessive inherited disorder characterized by prolonged partial thromboplastin time and absence of bleeding diathesis
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C537060Orphanet Code
ORPHA:483congenital high-molecular-weight kininogen deficiency
| MeSH | C537060 |
| Orphanet | ORPHA:483 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO