FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Meier-Gorlin syndrome 2 ID (Ontology) DOID:0080513 (Human Disease)
Definition A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC4 gene on chromosome 2q23.
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       1
Human Disease Models (FBhh)  DOID       1
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 Alleles Genes Human Disease Models
 Meier-Gorlin syndrome 2       1      1      1
 for disease ribbon | Meier-Gorlin syndrome 2       --       1       --
 model of | Meier-Gorlin syndrome 2       1      1       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
syndrome                         |
 |__Meier-Gorlin syndrome________|
                                 Meier-Gorlin syndrome 2  3 rec.
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Is a autosomal recessive disease
Meier-Gorlin syndrome
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MIM:613800