Panel | Mode of inheritance | Details |
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1 panel | ||
Green in Corneal dystrophyR-numbers: R262 Signed-off version 3.2 | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | Phenotypes Corneal dystrophy, Groenouw type I 121900, Corneal dystrophy, Avellino type 607541, Corneal dystrophy, Thiel-Behnke type 602082, Corneal dystrophy, lattice type I 122200, Corneal dystrophy, Reis-Bucklers type 608470, Corneal dystrophy, epithelial basement membrane 121820, Corneal dystrophy, lattice type IIIA 608471 |