raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:183634

Rare genetic parathyroid disease and phosphocalcic metabolism disorder

Type
Category
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRare genetic parathyroid disease and phosphocalcic metabolism disorder
frMaladie parathyroïdienne rare et anomalie du métabolisme phosphocalcique d'origine génétique
deNebenschilddrüsen- und Calcium/Phosphor-Stoffwechselkrankheiten, genetisch bedingte, seltene
esEnfermedad rara de la paratiroides y trastorno del metabolismo fosfocálcico de origen genético
itMalattia genetica rara delle paratiroidi con anomalie del metabolismo fosfocalcico
nlZeldzame genetische bijschildklierziekte en fosfocalcaire stofwisselingsstoornis
ptDoença da paratiroide e do metabolismo fosfo-cálcio genética rara
plRare genetic parathyroid disease and phosphocalcic metabolism disorder
csVzácná dědičná onemocnění příštítných tělísek a fosfokalciového metabolismu
ukРідкісне генетично обумовлене захворювання паращитовидної залози та порушення фосфокальцієвого обміну
zh罕见遗传性甲状旁腺疾病和钙磷代谢紊乱
trNadir genetik paratiroid hastalığı ve fosfokalsik metabolizma bozukluğu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15970Evalidated
UMLSC5680538Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (6):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

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

7

Sources for this card