raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3122

OBSOLETE: Sinus node disease-myopia syndrome

inactive · referred to ORPHA:166282Hereditary sick sinus syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Familial sick sinus syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Sinus node disease-myopia syndrome
frOBSOLETE : Syndrome de troubles du rythme-myopie
deOBSOLET: Sinusknoten-Syndrom und Myopie
esOBSOLETO: Síndrome de enfermedad del nodo sinusal-miopíaOBSOLETO: Alteraciones del ritmo cardíaco-miopía
itOBSOLETO: Disturbi del ritmo - miopia
nlOBSOLEET: Sinusknoopziekte - myopie-syndroom
ptOBSOLETO: Doença do nó sinusal-miopia
plNIEAKTUALNE: Choroba wezla zatokowego - miopia
csNEAKTUÁLNÍ: Syndrom sinusového uzlu a myopie
ukЗАСТАРІЛО: Синдром захворювання синусового вузла-міопії
zh弃用:窦房结病-近视综合征
trEski adı: Roussy-Lévy sendromu: Sinüs düğümü hastalığı-miyopi 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