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DO Term : pseudohypoparathyroidism type 1C [DOID:0051013] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A pseudohypoparathyroidism that has_material_basis_in a heterozygous mutation on the maternal allele of the GNAS gene on chromosome 20q13.
  • synonyms:
  • 612462,
  • ORDO:79444,
  • OMIM:612462,
  • GARD:10681,
  • PHP Ic
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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