| Db | Link | Name | Definition | Comment | Is a |
|---|---|---|---|---|---|
| HPO | HP:0000006 | Autosomal dominant inheritance | "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators] | — | HP:0000005 |
| HPO | HP:0011003 | High myopia | "A severe form of myopia with greater than -6.00 diopters." [DDD:ncarter] | — | HP:0000545 |
| OMIM | OMIM:614167 | MYOPIA 21, AUTOSOMAL DOMINANT; MYP21 | — | — | — |