Search Ontology:
Human Disease

primary autosomal recessive microcephaly 25

Term ID
DOID:0051036
Synonyms
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models