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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: MKS1, Meckel-Gruber syndrome, type 1,
Xenbase Genes : mks1
MONDO:0009571 - Meckel syndrome, type 1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Meckel syndrome (is_a)