Lisch epithelial corneal dystrophy
Synonyms: Band-shaped and whorled microcystic dystrophy of the corneal epithelium · LECD
- Type
- Disease
- Group
- Disorder
- Inheritance
- X-linked dominant
- Age of onset
- Childhood
- Status
- active
Lisch epithelial corneal dystrophy (LECD) is a very rare form of superficial corneal dystrophy characterized by feather-shaped opacities and microcysts in the corneal epithelium arranged in a band-shaped and sometimes whorled pattern, occasionally with impaired vision.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Lisch epithelial corneal dystrophy | Band-shaped and whorled microcystic dystrophy of the corneal epithelium · LECD |
| fr | Dystrophie cornéenne de Lisch | LECD |
| de | Lisch-epitheliale Hornhautdystrophie | |
| es | Distrofia corneal epitelial de Lisch | Distrofia microquística en forma de banda y verticilada del epitelio corneal · LECD |
| it | Distrofia corneale epiteliale di Lisch | Distrofia microcistica a bande dell'epitelio corneale · LECD |
| nl | Epitheliale corneadystrofie van Lisch | Bandvormige en gedraaide microcystische dystrofie van hoornvliesepitheel · LECD |
| pt | Distrofia corneana, tipo Lisch | |
| pl | Dystrofia nabłonkowa rogówki Lischa | LECD · Mikrotorbielowata dystrofia nabłonka rogówki o chrakterze smug i wirów |
| cs | Lischova epiteliální dystrofie rohovky | Pruhovitá a závitovitá mikrocystická dystrofie rohovkového epitelu · LECD |
| uk | Епітеліальна дистрофія рогівки Ліша | Стрічкоподібна та звивиста мікрокістозна дистрофія епітелію рогівки · LECD |
| zh | Lisch上皮细胞角膜营养不良 | 带状及螺旋状微囊性角膜上皮营养不良 |
| tr | Lisch epitel kornea distrofisi | LECD · Kornea epitelinin bant şeklinde ve kıvrımlı mikrokistik distrofisi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 620763 | E | validated | |
| ICD-10 | H18.5 | NTBT | attributed | validated |
| ICD-11 | 9A70.Y | NTBT | index | validated |
| MONDO | 0010425 | E | validated | |
| MeSH | C567588 | E | validated | |
| UMLS | C2749050 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:522562Genetic superficial corneal dystrophy
rare genetic diseases - ORPHA:98625Superficial corneal dystrophy
rare ophthalmic disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 36 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98955
- This record as JSON: /data/d/98955.json