FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term primary autosomal recessive microcephaly 16 ID (Ontology) DOID:0070289 (Human Disease)
Definition A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the ANKLE2 gene on chromosome 12q24.
Also Known As "MCPH16"
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DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      12
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 primary autosomal recessive microcephaly 16      13      4      1
 ameliorates | primary autosomal recessive microcephaly 16       3       --       --
 for disease ribbon | primary autosomal recessive microcephaly 16       --       1       --
 model of | primary autosomal recessive microcephaly 16      10      1       --
Spanning Tree (Parents/Children)
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autosomal recessive disease__
primary microcephaly_________|
                             primary autosomal recessive microcephaly
                              |__primary autosomal recessive microcephaly 16  18 rec.
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Is a primary autosomal recessive microcephaly
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Synonyms
  • "MCPH16" EXACT OMO:0003012
Secondary IDs
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MIM:616681