ORPHA:217467
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Also called Hereditary thrombophilia due to congenital HRG deficiency
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:217467 is classified under "Bone diseases" in the Orphanet nomenclature.