Disease #00463 (CDTB;CDB2 (dystrophy, corneal, Thiel-Behnke type (CDTB, corneal dystrophy of Bowman layer type2 (CDB-2))), OMIM:602082)
Official abbreviation |
CDTB;CDB2 |
Name |
dystrophy, corneal, Thiel-Behnke type (CDTB, corneal dystrophy of Bowman layer type2 (CDB-2)) |
OMIM ID |
602082 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
5 |
Phenotype entries for this disease |
4 |
Associated with 1 gene |
TGFBI |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-07-21 14:36:45 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|