FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term pseudohypoparathyroidism type 1C ID (Ontology) DOID:0051013 (Human Disease)
Definition A pseudohypoparathyroidism that has_material_basis_in a heterozygous mutation on the maternal allele of the GNAS gene on chromosome 20q13.
Also Known As "PHP Ic"
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DO.org
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 Genes
 pseudohypoparathyroidism type 1C       2
 for disease ribbon | pseudohypoparathyroidism type 1C       2
 model of | pseudohypoparathyroidism type 1C       2
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  metal metabolism disorder
   |__pseudohypoparathyroidism
       |__pseudohypoparathyroidism type 1C  2 rec.
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Synonyms
  • "PHP Ic" EXACT OMO:0003012
Secondary IDs
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GARD:10681
MIM:612462
ORDO:79444