Corneal dystrophy, subepithelial mucinous

Preferred Label : Corneal dystrophy, subepithelial mucinous;

Symbol : SMCD;

CISMeF acronym : SMCD;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Subepithelial mucinous corneal dystrophy;

Inheritance : Autosomal dominant;

Prefixed ID : 612867;

Details

Origin ID

612867;

UMLS CUI

C2748503;

Automatic exact mappings (from CISMeF team)
- Systemic mastocytosis [ICD-11 Subcategory]
Currated CISMeF NLP mapping
- Subepithelial mucinous corneal dystrophy [ICD-11 More detail]
- Subepithelial mucinous corneal dystrophy [ORDO Disease]
- Subepithelial mucinous corneal dystrophy (disorder) [SNOMED CT concept]
- corneal dystrophy, subepithelial mucinous [MeSH concept]
- corneal dystrophy, subepithelial mucinous [MeSH Supplementary Concept]
- subepithelial mucinous corneal dystrophy [DO Concept]
DO Cross reference
- subepithelial mucinous corneal dystrophy [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Corneal dystrophy [HPO term]
- Progressive visual loss [HPO term]
ORDO concept(s)
- Subepithelial mucinous corneal dystrophy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Subepithelial mucinous corneal dystrophy [ORDO Disease]
- Subepithelial mucinous corneal dystrophy (disorder) [SNOMED CT concept]
- corneal dystrophy, subepithelial mucinous [MeSH Supplementary Concept]
- corneal dystrophy, subepithelial mucinous [MeSH concept]
- subepithelial mucinous corneal dystrophy [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients