bn:02883518n
Noun Concept
Categories: Genodermatoses, Autosomal dominant disorders, Rare diseases, Wikipedia articles incorporating text from the 20th edition of Gray's Anatomy (1918), Diseases named for discoverer
EN
Albright's hereditary osteodystrophy  AHO-PHP syndrome Ia  Albright hereditary osteodystrophy  Albright hereditary osteodystrophy-PHP syndrome Ia  Albright Hereditary Osteodystrophy With Multiple Hormone Resistance
EN
Albright's hereditary osteodystrophy is a form of osteodystrophy, and is classified as the phenotype of pseudohypoparathyroidism type 1A; this is a condition in which the body does not respond to parathyroid hormone. Wikipedia
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EN
Albright's hereditary osteodystrophy is a form of osteodystrophy, and is classified as the phenotype of pseudohypoparathyroidism type 1A; this is a condition in which the body does not respond to parathyroid hormone. Wikipedia
Osteochondrodysplasia that has material basis in lack of responsiveness to parathyroid hormone which results in shortening and widening of long bones of the located in hand or located in foot along with short stature, obesity, and rounded face Wikidata
A form of osteodystrophy, classified as the phenotype of pseudohypoparathyroidism type 1A. Wiktionary