FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term adult hypophosphatasia ID (Ontology) DOID:0110913 (Human Disease)
Definition A hypophosphatasia that has_material_basis_in a heterozygous or compound heterozygous mutation of the ALPL gene on chromosome 1p36.12.
Also Known As "mild hypophosphatasia"
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DO.org
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 Genes
 adult hypophosphatasia       7
 for disease ribbon | adult hypophosphatasia       7
 model of | adult hypophosphatasia       7
Spanning Tree (Parents/Children)
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autosomal genetic disease__
syndrome___________________|
                           hypophosphatasia
                            |__adult hypophosphatasia  7 rec.
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Is a hypophosphatasia
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Synonyms
  • "mild hypophosphatasia" EXACT
Secondary IDs
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MIM:146300
ORDO:247676