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Disease Ontology Browser
Meckel syndrome 7 (DOID:0070121)
Alliance: disease page
Synonyms: Meckel-Gruber syndrome, type 7; MKS7
Alt IDs: OMIM:267010, MESH:C537756, ORDO:3032, UMLS_CUI:C2673885
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of NPHP3 on chromosome 3q22.1.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory