Type I lattice corneal dystrophy (LCDI) is a frequent form of stromal corneal dystrophy (see this term) characterized by a network of delicate interdigitating branching filamentous opacities within the cornea with progressive visual impairment and no systemic manifestations.
Synonyms: Biber-Haab-Dimmer dystrophy Classic lattice corneal dystrophy LCD1 Lattice corneal dystrophy type 1 LCDI
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Term information
database cross reference
- OMIM:122200 (E (Exact mapping: the two concepts are equivalent))
- UMLS:C2931650 (E (Exact mapping: the two concepts are equivalent))
- OMIM:608471 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- MeSH:C537881 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:H18.5 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- ICD-10:H18.5 (Attributed (The ICD10 code is attributed by Orphanet))
- UMLS:C1690006 (E (Exact mapping: the two concepts are equivalent))
Term relations
Subclass of:
- disease
- present_in some Worldwide and has_point_prevalence_range some Unknown_epidemiological_range
- part_of some Stromal corneal dystrophy
- has_inheritance some autosomal dominant
- has_age_of_onset some all ages