Albright's hereditary osteodystrophy
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
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Albright's hereditary osteodystrophy
Summary
Albright's hereditary osteodystrophy is a rare disease[1]. It draws 7 Wikipedia views per month (rare_disease category, ranking #231 of 627).[2]
Key Facts
- Albright's hereditary osteodystrophy's instance of is recorded as rare disease[3].
- Albright's hereditary osteodystrophy's instance of is recorded as class of disease[4].
- Albright's hereditary osteodystrophy's subclass of is recorded as pseudohypoparathyroidism[5].
- Albright's hereditary osteodystrophy's subclass of is recorded as pseudohypoparathyroidism with Albright hereditary osteodystrophy[6].
- Albright's hereditary osteodystrophy's OMIM ID is recorded as 103580[7].
- Albright's hereditary osteodystrophy's ICD-9 ID is recorded as 275.49[8].
- Albright's hereditary osteodystrophy's ICD-10 ID is recorded as E20.1[9].
- Albright's hereditary osteodystrophy's DiseasesDB is recorded as 10835[10].
- Albright's hereditary osteodystrophy's Disease Ontology ID is recorded as DOID:0080053[11].
- Albright's hereditary osteodystrophy's Gran Enciclopèdia Catalana ID is recorded as 0061533[12].
- Albright's hereditary osteodystrophy's described by source is recorded as Gray's Anatomy (20th edition)[13].
- Albright's hereditary osteodystrophy's Orphanet ID is recorded as 79443[14].
- Albright's hereditary osteodystrophy's Orphanet ID is recorded as 665[15].
- Albright's hereditary osteodystrophy's ICD-9-CM is recorded as 275.49[16].
- Albright's hereditary osteodystrophy's NCI Thesaurus ID is recorded as C118434[17].
- Albright's hereditary osteodystrophy's NCI Thesaurus ID is recorded as C129721[18].
- Albright's hereditary osteodystrophy's health specialty is recorded as endocrinology[19].
- Albright's hereditary osteodystrophy's genetic association is recorded as GNAS[20].
- Albright's hereditary osteodystrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080053[21].
- Albright's hereditary osteodystrophy's exact match is recorded as http://identifiers.org/doid/DOID:0080053[22].
- Albright's hereditary osteodystrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_665[23].
- Albright's hereditary osteodystrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79443[24].
- Albright's hereditary osteodystrophy's UMLS CUI is recorded as C3494506[25].
- Albright's hereditary osteodystrophy's UMLS CUI is recorded as C0033806[26].
- Albright's hereditary osteodystrophy's Medical Dictionary for Regulatory Activities ID is recorded as 10037126[27].
Why It Matters
Albright's hereditary osteodystrophy draws 7 Wikipedia views per month (rare_disease category, ranking #231 of 627).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] It is known by 17 alternative names across languages and contexts.[29]