eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | albright hereditary osteodystrophy |
| Comorbidity | C0033806|pseudohypoparathyroidism type ia |
| Sentences | 1 |
| PubMedID- 25802881 | Maternally inherited inactivating gnas mutations are the most common cause of parathyroid hormone (pth) resistance and albright hereditary osteodystrophy (aho) leading to pseudohypoparathyroidism type ia (phpia) due to gsalpha deficiency. |
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