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Pseudopseudohypoparathyroidism
rareA disease characterized by a constellation of clinical features collectively termed Albright hereditary osteodystrophy (AHO) but no evidence of resistance to parathyroid hormone (PTH), which is seen in other forms of pseudohypoparathyroidism (PHP).
- Identifiers
- MONDO:0012912 OMIM:612463Orphanet:665Orphanet:79445
- Causal genes
- GNAS
- Also known as
- aho-PPHP syndrome · Albright hereditary osteodystrophy-PPHP syndrome · Normocalcemic pseudohypoparathyroidism (disorder) [ambiguous] · PPHP · pseudo-pseudohypoparathyroidism
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