Search Ontology:
Human Disease
primary autosomal recessive microcephaly 25
- Term ID
- DOID:0051036
- Synonyms
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- Definition
- A primary autosomal recessive microcephaly that has_material_basis_in homozygous mutation in the MAP11 gene on chromosome 7q22. https://pubmed.ncbi.nlm.nih.gov/30715179/
- References
- Ontology
- Human Disease ( DOID:0051036 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models