hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

MeSH: C567737ORPHA: 217467

Overview

human disease

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

C567737

Orphanet Code

ORPHA:217467
hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
MeSHC567737
OrphanetORPHA:217467
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO