raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:99179

Kandori fleck retina

Type
Malformation syndrome
Group
Disorder
Age of onset
Adolescent, Adult, Childhood
Status
active

Kandori fleck retina is a rare, genetic retinal dystrophy disorder characterized by irregular, sharply defined, yellowish-white lesions of variable size that are distributed mainly in the nasal equatorial region of the retina, with a tendency to confluence, that are not associated with any vascular or optic nerve abnormalities. They frequently manifest as mild and stationary night blindness.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enKandori fleck retina
frDystrophie de Kandori
deGefleckte Retina nach Kandori
esRetina moteada de Kandori
itRetina a chiazze, tipo Kandori
nlFleck retina van Kandori
ptRetina mosqueada de Kandori
plplamkowata siatkówka Kandori
csKandoriho skvrnitá sítnice
ukСітківка з плямами Кандори
zhKandori斑点样视网膜
trKandori benekli retina

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM228990Evalidated
ICD-10H35.5NTBTattributedvalidated
ICD-119B70NTBTindexvalidated
MONDO0009236Evalidated
MeSHC562701Evalidated
UMLSC0271257Evalidated

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

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