Albright's Hereditary Osteodystrophy
What's New
Last Posted: Mar 10, 2023
- Clinical and genetic characteristics of Pseudohypoparathyroidism in the Chinese population.
Chu Xueying, et al. Clinical endocrinology 2017 0 (2) 285-294 - Obesity-Associated GNAS Mutations and the Melanocortin Pathway.
Mendes de Oliveira Edson et al. The New England journal of medicine 2021 - No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity.
Izzi Benedetta, et al. Journal of human genetics 2012 4 (4) 277-9 - Albright's hereditary osteodystrophy
From NCATS Genetic and Rare Diseases Information Center
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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