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Echinobase
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,

Echinobase Genes :


OMIM:
MIM:257320 - lissencephaly 2; lis2

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

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