Please sign in to follow a disease.

Carboxypeptidase N deficiency

MONDO:0008910

An autosomal recessive condition caused by mutation(s) in the CPN1 gene, encoding carboxypeptidase N catalytic chain. It may be characterized by episodic angioedema, chronic urticaria, asthma and/or allergic hypersensitivity.

Also known as: carboxypeptidase N deficiency

0 clinical trials for this condition and its sub-types, 0 tagged with Carboxypeptidase N deficiency itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary disease (18235)

Including sub-types (0) Tagged with Carboxypeptidase N deficiency (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.