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Summary Literature (0)
MIM:267010 - MECKEL SYNDROME, TYPE 7; MKS7

Xenbase Genes: nphp3

Human Disease Resource: OMIM

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

Disease Ontology (DO):
DOID:0070121 - Meckel syndrome 7