Cytoscape Web
Click node...

Meesmann corneal dystrophy
1 OMIM reference -
2 associated genes
12 connected diseases
No signs/symptoms info
Disease Type of connection
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex, Dowling-Meara type
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
Localized epidermolysis bullosa simplex
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Opsismodysplasia
Autosomal recessive epidermolysis bullosa simplex
Dermatopathia pigmentosa reticularis
Dowling-Degos disease
Epidermolysis bullosa simplex with circinate migratory erythema
Naegeli-Franceschetti-Jadassohn syndrome
Synonym(s):
- Juvenile hereditary epithelial dystrophy of Meesmann
- MECD
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: D053559
Gene symbol UniProt reference OMIM reference
KRT12 Q99456601687
KRT3 P12035148043
No signs/symptoms info available.