FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Warburg micro syndrome 3 ID (Ontology) DOID:0110718 (Human Disease)
Definition A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB18 gene on chromosome 10p12.
Also Known As "Micro Syndrome 3" ; "WARBM3"
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 Genes
 Warburg micro syndrome 3       1
 for disease ribbon | Warburg micro syndrome 3       1
 model of | Warburg micro syndrome 3       1
Spanning Tree (Parents/Children)
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autosomal recessive disease__
syndrome_____________________|
                             Warburg micro syndrome
                              |__Warburg micro syndrome 3  1 rec.
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Is a Warburg micro syndrome
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Synonyms
  • "Micro Syndrome 3" EXACT
    "WARBM3" EXACT OMO:0003012
Secondary IDs
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ICD10CM:Q87.0
MIM:614222