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Echinobase
Summary Literature (0)
DOID:0070115 - Meckel syndrome 1

Disease Ontology Definition:A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the MKS1 gene on chromosome 17q22.

Synonyms: Meckel-Gruber syndrome, type 1, MKS1

Echinobase Genes : mks1


MIM:
MIM:249000 - meckel syndrome, type 1; mks1

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

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