Disease #02176 (deficiency, phosphoglycerate kinase 1, OMIM:300653)

Official abbreviation -
Name deficiency, phosphoglycerate kinase 1
OMIM ID 300653
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PGK1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A