Hereditary corneal dystrophies

Preferred Label : Hereditary corneal dystrophies;

Associé à un acte opératoire (%) : 85.0;

Diag associé à un acte (%) : 96.3;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

H185;

UMLS CUI

C0010035;

Automatic exact mappings (from CISMeF team)
- Hereditary corneal dystrophies [ICD-9 code]
Currated CISMeF NLP mapping
- Hereditary Corneal Dystrophy [NCIt concept]
- Hereditary corneal dystrophies [ICD-10 Sub-category (who)]
- Hereditary corneal dystrophies [ICD-11 Category]
- Hereditary corneal dystrophy (disorder) [SNOMED CT concept]
- corneal dystrophies, hereditary [MeSH Descriptor]
- corneal dystrophies, hereditary [MeSH concept]
- hereditary cornea dystrophy [Disease (Nov.)]
- hereditary corneal dystrophy, nos [SNOMED Notion]
DO Cross reference
- Lisch epithelial corneal dystrophy [DO Concept]
- X-linked endothelial corneal dystrophy [DO Concept]
- congenital stromal corneal dystrophy [DO Concept]
- corneal dystrophy [DO Concept]
- epithelial basement membrane dystrophy [DO Concept]
- posterior amorphous corneal dystrophy [DO Concept]
- posterior polymorphous corneal dystrophy [DO Concept]
- subepithelial mucinous corneal dystrophy [DO Concept]
Orphanet concepts
- Central cloudy dystrophy of François [ORDO Disease]
- Central discoid corneal dystrophy [ORDO Disease]
- Climatic droplet keratopathy [ORDO Disease]
- Congenital hereditary endothelial dystrophy type I [ORDO Disease]
- Congenital hereditary endothelial dystrophy type II [ORDO Disease]
- Congenital stromal corneal dystrophy [ORDO Disease]
- Corneal dystrophy [ORDO Disease]
- Corneal dystrophy-perceptive deafness syndrome [ORDO Disease]
- Corneodermatoosseous syndrome [ORDO Disease]
- Epithelial basement membrane dystrophy [ORDO Disease]
- Epithelial recurrent erosion dystrophy [ORDO Disease]
- Fleck corneal dystrophy [ORDO Disease]
- Fuchs endothelial corneal dystrophy [ORDO Disease]
- Gelatinous drop-like corneal dystrophy [ORDO Disease]
- Granular corneal dystrophy type I [ORDO Disease]
- Granular corneal dystrophy type II [ORDO Disease]
- Grayson-Wilbrandt corneal dystrophy [ORDO Disease]
- Lattice corneal dystrophy type I [ORDO Disease]
- Lisch epithelial corneal dystrophy [ORDO Disease]
- Macular corneal dystrophy [ORDO Disease]
- Meesmann corneal dystrophy [ORDO Disease]
- Posterior amorphous corneal dystrophy [ORDO Disease]
- Posterior corneal dystrophy [ORDO Disease]
- Posterior polymorphous corneal dystrophy [ORDO Disease]
- Pre-Descemet corneal dystrophy [ORDO Disease]
- Reis-Bücklers corneal dystrophy [ORDO Disease]
- Schnyder corneal dystrophy [ORDO Disease]
- Stromal corneal dystrophy [ORDO Disease]
- Subepithelial mucinous corneal dystrophy [ORDO Disease]
- Superficial corneal dystrophy [ORDO Disease]
- Thiel-Behnke corneal dystrophy [ORDO Disease]
- X-linked endothelial corneal dystrophy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary Corneal Dystrophy [NCIt concept]
- Hereditary corneal dystrophies [ICD-9 code]
- Hereditary corneal dystrophies [ICD-11 Category]
- Hereditary corneal dystrophy (disorder) [SNOMED CT concept]
- Hereditary corneal dystrophy, unspecified [MedDRA LLT]
- Hereditary corneal dystrophy, unspecified [ICD-9 code]
- corneal dystrophies, hereditary [MeSH Descriptor]
- corneal dystrophies, hereditary [MeSH concept]
- hereditary cornea dystrophy [Disease (Nov.)]
- hereditary corneal dystrophy, nos [SNOMED Notion]

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