dermochondrocorneal dystrophy of françois

Preferred Label : dermochondrocorneal dystrophy of françois;

MeSH synonym : francois syndrome; dermochondrocorneal dystrophy;

Origin ID

C535375;

UMLS CUI

C0432288;

Automatic exact mappings (from CISMeF team)
- Dermochondrocorneal dystrophy of François [PASCAL descriptor]
CISMeF manual mappings
- Dermochondrocorneal dystrophy [ORDO Disease]
Currated CISMeF NLP mapping
- Dermochondrocorneal dystrophy [ICD-11 More detail]
- Dermochondrocorneal dystrophy [OMIM Phenotype]
- Francois syndrome (disorder) [SNOMED CT concept]
- dermochondrocorneal dystrophy [Disease (Nov.)]
MeSH term(s) associated for indexing
- corneal dystrophies, hereditary [MeSH Descriptor]
- exostoses, multiple hereditary [MeSH Descriptor]
ORDO relation(s)
- Dermochondrocorneal dystrophy [ORDO Disease]
Record concept(s)
- Dermochondrocorneal dystrophy of François [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dermochondrocorneal dystrophy [OMIM Phenotype]
- Dermochondrocorneal dystrophy [ORDO Disease]
- Francois syndrome (disorder) [SNOMED CT concept]
- dermochondrocorneal dystrophy [Disease (Nov.)]