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PLG-related hereditary angioedema with normal C1Inh
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ORPHA:537072
Summary
An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.
Detailed information
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
Guidelines
Emergency guidelines
Clinical practice guidelines
Diagnostic Keys
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
- Research project(s) (35)
- Clinical trial(s) (5)
- Biobank(s) (8)
- Registry(ies) (24)
- Network of experts (4)
Newborn screening
The documents contained in this website are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.