Disease #01721 (CHED (dystrophy, corneal, endothelial), OMIM:217700)
Official abbreviation |
CHED |
Name |
dystrophy, corneal, endothelial |
OMIM ID |
217700 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
46 |
Phenotype entries for this disease |
16 |
Associated with 1 gene |
SLC4A11 |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2023-03-22 16:48:05 +01:00 (CET) |
Individuals
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