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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/615946
http://purl.bioontology.org/ontology/OMIM/615946
|
|---|---|
| Preferred Name | MYOPIA 24, AUTOSOMAL DOMINANT |
| Synonyms |
MYP24
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | MYP24
|
|---|---|
| prefLabel | MYOPIA 24, AUTOSOMAL DOMINANT
|
| Gene Symbol |
SLC39A5
MYP24
|
| Scope Statement | Caused by mutation in the member 5 solute carrier family 39 (zinc transporter) gene (SLC39A5, 608730.0001) [MOLECULAR BASIS]
Onset before 10 years of age in all patients [MISCELLANEOUS]
|
| type | |
| Has manifestation | |
| tui | T047
|
| Gene Locus | 12q13.3
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 615946
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C4014762
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |