Neu-Laxova syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Neu-Laxova syndrome (NLS) is a rare, multiple malformation syndrome characterised by severe intrauterine growth retardation (IUGR), severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism. (Orphanet Rare Disease Ontology, Orphanet_2671)
External Link http://www.omim.org/entry/256520
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Genes

1 genes associated with the Neu-Laxova syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
PHGDH phosphoglycerate dehydrogenase