raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:140286

Secondary hypoparathyroidism due to impaired parathormon secretion

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
Adolescent, Adult, Childhood, Elderly
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enSecondary hypoparathyroidism due to impaired parathormon secretion
frHypoparathyroïdie secondaire due à un défaut de sécrétion de parathormone
deHypoparathyreoidismus durch gestörte Parathormon-Sekretion, sekundärer
esHipoparatiroidismo secundario por una secreción deficiente de paratohormona
itIpoparatiroidismo secondario da deficit di secrezione del paratormone
nlSecundaire hypoparathyreoïdie door verminderde parathormoonsecretie
ptHipoparatiroidismo por secreção reduzida da paratormona, secundária
plWtórna niedoczynność przytarczyc z powodu upośledzonego wydzielania parathormonu
csSekundární hypoparatyreóza způsobená poruchou sekrece parathormonu
ukВторинний гіпопаратиреоз внаслідок порушення секреції паратгормону
zh甲状旁腺激素分泌受损所致继发性甲状旁腺功能减退
trBozulmuş parathormon sekresyonuna bağlı sekonder hipoparatiroidi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10E20.8NTBTattributedvalidated
ICD-115A50.01Especificvalidated
MONDO0015357Evalidated
UMLSC4305428Evalidated
GARD19922Evalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

4 records
TypeClassValueAreaQualificationValidationSource
Point prevalence1-5 / 10 00024.75 / 100 000EuropeValue and classValidated29087618[PMID]_23661265[PMID]_29516129[PMID]_30375660[PMID]
Annual incidenceUnknown—EuropeClass onlyValidatedORPHANET
Annual incidence1-9 / 1 000 0000.8 / 100 000DenmarkValue and classValidated23661265[PMID]
Annual incidence1-9 / 100 0001.7 / 100 000SpainValue and classValidated32155210[PMID]

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

26 annotations · validated 2024-07-01
HPOTerm (as annotated by Orphanet)Diagnostic
Very frequent (99-80%)
HP:0000828Abnormality of the parathyroid gland
Frequent (79-30%)
HP:0002135Basal ganglia calcification
HP:0031817Decreased circulating parathyroid hormone level
HP:0012378Fatigue
HP:0002905Hyperphosphatemia
HP:0002901Hypocalcemia
HP:0000829Hypoparathyroidism
HP:0000121Nephrocalcinosis
Occasional (29-5%)
HP:0031006Acroparesthesia
HP:0000739Anxiety
HP:0011675Arrhythmia
HP:0007302Bipolar affective disorder
HP:0033630Brain fog
HP:4000007Bronchoconstriction
HP:0031990Chvostek sign
HP:0000716Depression
HP:0002380Fasciculations
HP:0002150Hypercalciuria
HP:0033748Hypoesthesia
HP:0025425Laryngospasm
HP:0003394Muscle spasm
HP:0002749Osteomalacia
HP:0007787Posterior subcapsular cataract
HP:0002748Rickets
HP:0001250Seizure
HP:6000919Trousseau sign

Run the differential on the 1 obligate / very frequent terms

Annotation source: 28722928[PMID]_22863393[PMID]_26943720[PMID]

7

Sources for this card