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
|