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DOID:0060469 - Miller-Dieker lissencephaly syndrome
Disease Ontology Definition:A syndrome characterized by classical lissencephaly and distinct facial features and has_material_basis_in submicroscopic deletions of 17p13.3, including the LIS1 gene.
Synonyms: MDS, Miller-Dieker syndrome
Xenbase Genes
:
ywhae,
pafah1b1
| MONDO:0009532 - Miller-Dieker lissencephaly syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
syndrome (is_a)