raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98995

Early-onset zonular cataract

Type
Clinical subtype
Group
Subtype of disorder
Inheritance
Autosomal dominant, Autosomal recessive, X-linked recessive
Age of onset
Infancy, Neonatal
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enEarly-onset zonular cataract
frCataracte zonulaire précoce
deKatarakt, zonuläre, früh-beginnende
esCatarata zonular de inicio precoz
itCataratta zonulare a esordio precoceCataratta lamellare
nlZonulair cataract met vroege aanvang
ptCatarata zonular de início precoce
plZaćma strefowa o wczesnym początku
csZonulární katarakta s časným nástupem
ukРання зональна катаракта
zh早发性绕核性白内障
trErken başlangıçlı zonüler katarakt
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM116400BTNTvalidated
OMIM605728BTNTvalidated
OMIM607304BTNTvalidated
OMIM609376BTNTvalidated
OMIM610019BTNTvalidated
OMIM613763BTNTvalidated
ICD-10Q12.0NTBTattributedvalidated
ICD-11LA12.1NTBTindexvalidated
MONDO0020379Evalidated
MeSHC535342Evalidated
UMLSC5681642Evalidated
GARD1898Evalidated

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 (3):

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