Term Name:	Neu-Laxova syndrome 2
Synonyms:
Definition:	A serine deficiency that is characterized by multiple fatal malformations including ichthyosis, microcephaly, central nervous system abnormalities, limb deformities, intrauterine growth restriction, proptosis, anasarca, and micrognathia, and has_material_basis_in autosomal recessive inheritance of mutation in the PSAT1 gene on chromosome 9q21.1, causing issues producing the amino acid serine.
Ontology:	Human Disease [DOID:0080075]   ( DOID:0080075 )