Search Ontology:
Human Disease
primary autosomal recessive microcephaly 3
- Term ID
- DOID:0070286
- Synonyms
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- MCPH3
- Definition
- A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CDK5RAP2 gene on chromosome 9q33. https://www.ncbi.nlm.nih.gov/pubmed/15793586
- References
- Ontology
- Human Disease ( DOID:0070286 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models