Early-onset lamellar cataract

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Early-onset lamellar cataract

ORPHA:441452Clinical subtype

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Inheritance
Autosomal dominant
Classified as
Clinical subtype

Recorded for the broader condition

Age of onset
Infancy, NeonatalEarly-onset zonular cataract

Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.

Genes

BFSP2Disease-causing germline mutation(s)
CRYAADisease-causing germline mutation(s)
CRYABDisease-causing germline mutation(s)
CRYBA1Disease-causing germline mutation(s)
CRYBA4Disease-causing germline mutation(s)
CRYGBDisease-causing germline mutation(s)
CRYGCDisease-causing germline mutation(s)
CRYGDDisease-causing germline mutation(s)
CRYGSDisease-causing germline mutation(s)
HSF4Disease-causing germline mutation(s)
MIPDisease-causing germline mutation(s)

ICD-10 codes

H26.8filed under a broader ICD-10 category

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

MONDO 0018611OMIM 116100OMIM 600881OMIM 613763UMLS C5681191

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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