serine deficiency

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Summary

Literature (0)

DOID:0050721 - serine deficiency

Disease Ontology Definition:An amino acid metabolic disorder that has_material_basis_in defects in the biosynthesis of the amino acid L-serine.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: psph, psat1, phgdh

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0000421 - inborn serine deficiency

MONDO:0000421 - inborn serine deficiency

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): amino acid metabolic disorder (is_a)