Disease #05698 (HMNDYT2 (hypermanganesemia with dystonia, type 2 (HMNDYT2)), OMIM:617013)
| Official abbreviation |
HMNDYT2 |
| Name |
hypermanganesemia with dystonia, type 2 (HMNDYT2) |
| OMIM ID |
617013 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
SLC39A14 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-02-22 09:39:43 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
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