raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:263417

Bartter syndrome with hypocalcemia

inactive · moved to ORPHA:428Autosomal dominant hypocalcemia

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Autosomal dominant hypocalcemia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enBartter syndrome with hypocalcemia
frSyndrome de Bartter avec hypocalcémie
deBartter-Syndrom mit Hypokalzämie
esSíndrome de Bartter con hipocalcemia
itSindrome di Bartter con ipocalcemiaSindrome di Bartter, tipo 5 · Sindrome di Bartter, tipo V
nlSyndroom van Bartter met hypocalciëmie
ptSíndrome de Bartter com hipocalcémia
plZespół Barttera z hipokalcemiąZespół Barttera typu 5 · Zespół Barttera typu V
csBartterův syndrom s hypokalcémiíBartterův syndrom, typ 5 · Bartterův syndrom, typ V
ukСиндром Барттера з гіпокальціємією
zh巴特综合征伴低钙血症
trHipokalsemi ile seyreden Bartter sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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