FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary spastic paraplegia 72A ID (Ontology) DOID:0110817 (Human Disease)
Definition A hereditary spastic paraplegia that has_material_basis_in a heterozygous mutation in the REEP2 gene on chromosome 5q31.2.
Also Known As "SPG72"
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 Genes
 hereditary spastic paraplegia 72A       1
 for disease ribbon | hereditary spastic paraplegia 72A       1
 model of | hereditary spastic paraplegia 72A       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 72A  1 rec.
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Is a autosomal dominant disease
hereditary spastic paraplegia
Part of
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Synonyms
  • "SPG72" EXACT OMO:0003012
Secondary IDs
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ICD10CM:G11.4
MIM:615625
ORDO:401849