Disease #02392 (PHGDHD (deficiency, phosphoglycerate dehydrogenase (PHGDHD)), OMIM:601815)

Official abbreviation PHGDHD
Name deficiency, phosphoglycerate dehydrogenase (PHGDHD)
OMIM ID 601815
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PHGDH
Associated tissues -
Disease features -
Remarks -