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DO Term : microcephaly and chorioretinopathy 2 [DOID:0080106] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
616171,
OMIM:616171

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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