raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98678

OBSOLETE: X-linked recessive optic atrophy

inactive · referred to ORPHA:98671Hereditary optic neuropathy

Type
Category
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 Hereditary optic neuropathy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: X-linked recessive optic atrophy
frOBSOLETE : Atrophie optique liée à l'X
deOBSOLET: Optikusatrophie, X-chromosomal-rezessive
esOBSOLETO: Atrofia óptica recesiva ligada al cromosoma X
itOBSOLETO: Atrofia ottica recessiva legata all'X
nlOBSOLEET: X-gebonden recessieve optische atrofie
ptOBSOLETO: Atrofia óptica recessiva ligada ao X
plNIEAKTUALNE: Recesywny zanik nerwu wzrokowego sprzezony z chromosomem X
csNEAKTUÁLNÍ: X-vázaná recesivní atrofie zrakového nervu
ukЗАСТАРІЛО: Х-зчеплена рецесивна атрофія зорового нерва
zh弃用:X-连锁隐性遗传视神经萎缩
trEski adı: X'e bağlı resesif optik atrofi
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