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Summary Literature (0)
DOID:0060902 - Norman-Roberts syndrome

Disease Ontology Definition:A lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22.

Synonyms: lissencephaly 2, lissencephaly syndrome, Norman-Roberts type

Xenbase Genes : reln

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009760 - Norman-Roberts syndrome

MIM:
MIM:257320 - LISSENCEPHALY 2; LIS2

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), lissencephaly (is_a)