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DO Term : pseudohypoparathyroidism type 1A [DOID:0080053] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A pseudohypoparathyroidism that characterized by shortening and widening of long bones located_in the hand or located_in the foot along with short stature, obesity, rounded face, and lack of responsiveness to parathyroid hormone that has_material_basis_in a mutation resulting in loss of function of the Gs-alpha isoform of the GNAS gene on the maternal allele. This results in expression of the Gs-alpha protein only from the paternal allele.
  • synonyms:
  • PHP Ia,
  • Albright's hereditary osteodystrophy,
  • ORDO:79443,
  • GARD:7486,
  • 103580,
  • Albright hereditary osteodystrophy,
  • OMIM:103580
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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents