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microcephaly and chorioretinopathy 2

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any microcephaly and chorioretinopathy in which the cause of the disease is a mutation in the PLK4 gene.
Uniprot Description A severe disorder characterized by microcephaly, delayed psychomotor development, growth retardation with dwarfism, and ocular abnormalities.
Mondo Term and Equivalent IDs
MONDO:0014516:  microcephaly and chorioretinopathy 2
UMLS:C4015388: