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Summary Literature (0)
DOID:0070121 - Meckel syndrome 7

Disease Ontology Definition:A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the NPHP3 gene on chromosome 3q22.1.

Synonyms: Meckel-Gruber syndrome, type 7, MKS7

Xenbase Genes : nphp3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009966 - NPHP3-related Meckel-like syndrome

MIM:
MIM:267010 - MECKEL SYNDROME, TYPE 7; MKS7

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)