Search Ontology:
Human Disease
primary autosomal recessive microcephaly 9
- Term ID
- DOID:0070292
- Synonyms
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- MCPH9
- Definition
- A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/20598275
- References
- Ontology
- Human Disease ( DOID:0070292 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models