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  • Disease Ontology Term: primary autosomal recessive microcephaly 25
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Disease Ontology Term: primary autosomal recessive microcephaly 25


DO ID
DOID:0051036
Description
A primary autosomal recessive microcephaly that has_material_basis_in homozygous mutation in the MAP11 gene on chromosome 7q22.
View DO Annotations for yeast and other model organisms at the Alliance of Genome Resources

Ontology Diagram


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Click on a Disease Ontology term to go to its specific page within SGD; drag any of the Disease Ontology term objects around within the visualization for easier viewing; click “Reset” to automatically redraw the diagram.

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Annotations


Manually Curated

There are no manually curated annotations for primary autosomal recessive microcephaly 25.

High-throughput

There are no high-throughput annotations for primary autosomal recessive microcephaly 25.

Computational

There are no computational annotations for primary autosomal recessive microcephaly 25.
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