ORPHA:457059

OBSOLETE: Pseudohypoparathyroidism with Albright hereditary osteodystrophy

inactive · referred to ORPHA:97593Pseudohypoparathyroidism

Type: Clinical group
Group: Group of disorders
Status: inactive
Flag: Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Pseudohypoparathyroidism

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Pseudohypoparathyroidism with Albright hereditary osteodystrophy
fr	OBSOLETE : Pseudohypoparathyroïdie avec ostéodystrophie héréditaire d'Albright
de	OBSOLET: Pseudohypothyreoidismus mit Albright'sche hereditäre Osteodystrophie
es	OBSOLETO: Pseudohipoparatiroidismo con osteodistrofia hereditaria de Albright
it	OBSOLETO: Pseudoipotiroidismo con osteodistrofia ereditaria di Albright
nl	OBSOLEET: Pseudo-hypoparathyreoïdie met hereditaire osteodystrofie van Albright
pt	OBSOLETO: Pseudo-hipoparatiroidismo com osteodistrofia hereditária de Albright
pl	NIEAKTUALNE: Rzekoma niedoczynność przytarczyc z dziedziczną osteodystrofią Albrighta
cs	NEAKTUÁLNÍ: Pseudohypoparathyreoidismus s Albrightovou hereditární osteodystrofií
uk	Псевдогіпопаратиреоз зі спадковою остеодистрофією Олбрайта
zh	假性甲状旁腺功能减退症合并奥尔布赖特遗传性骨发育不全
tr	Albright kalıtsal osteodistrofi ile seyreden psödohipoparatiroidi

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Not placed in any Orphanet classification in this release.

No children.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/457059
This record as JSON: /data/d/457059.json