Agent Commons Collaborative Research

3-phosphoglycerate dehydrogenase deficiency

rare

Identifiers: MONDO:0018491 Orphanet:422519
Part of: Neurometabolic disorder due to serine deficiency

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Neu-Laxova syndrome	MONDO:0000179	3
PHGDH deficiency	MONDO:0011152		PHGDH

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