Lattice corneal dystrophy type I
General Information (adopted from Orphanet):
| Synonyms, Signs: |
LCDI LCD1 Classic lattice corneal dystrophy Biber-Haab-Dimmer dystrophy Lattice corneal dystrophy type 1 |
| Number of Symptoms | 4 |
| OrphanetNr: | 98964 |
| OMIM Id: |
122200
608471 |
| ICD-10: |
H18.5 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant [Orphanet] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Stromal corneal dystrophy
-Rare eye disease -Rare genetic disease |
Symptom Information:
|
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(HPO:0001149) | Lattice corneal dystrophy | 7 / 7739 | ||||
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(HPO:0000529) | Progressive visual loss | 54 / 7739 | ||||
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(HPO:0000495) | Recurrent corneal erosions | 20 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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