raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:183607

Genetic lens and zonula anomaly

Type
Category
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enGenetic lens and zonula anomaly
frAnomalie génétique du cristallin et de la zonule
deLinsen/Zonula-Anomalie, genetisch bedingte
esAnomalía del cristalino y de la zónula de origen genético
itAnomalia genetica del cristallino e della zonula
nlGenetische lens- en zonula-anomalie
ptAnomalia genética do cristalino e zónula
plWada soczewek i obwódki rzęskowej uwarunkowana genetycznie
csGeneticky podmíněné anomálie čočky a zonuly
ukГенетично обумовлена аномалія кришталика та зонули
zh遗传性晶状体及睫状小带异常
trGenetik lens ve zonula anomalisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5680542Evalidated

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):

Children (6):

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