Search Ontology:
Human Disease

microcephaly and chorioretinopathy 2

Term ID
DOID:0080106
Synonyms
Definition
A syndrome that is characterized by delayed psychomotor development, visual impairment, and short stature and has_material_basis_in homozygous mutation in the PLK4 gene. https://www.ncbi.nlm.nih.gov/pubmed/25344692
References
Ontology
Human Disease   ( DOID:0080106 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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