Disease #02325 (Proprotein convertase 1/3 deficiency, OMIM:600955)

Official abbreviation -
Name Proprotein convertase 1/3 deficiency
OMIM ID 600955
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PCSK1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A