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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 MKS1 on chromosome 17q22.
Synonyms: MKS1, Meckel-Gruber syndrome, type 1,
Echinobase Genes : mks1
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)