Hypermanganesemia with dystonia 2

Definition

Any hypermanganesemia with dystonia in which the cause of the disease is a mutation in the SLC39A14 gene.

Also known as HMNDYT2, hypermanganesemia with dystonia 2, hypermanganesemia with dystonia 2; HMNDYT2, hypermanganesemia with dystonia caused by mutation in SLC39A14, hypermanganesemia with dystonia type 2, SLC39A14 hypermanganesemia with dystonia — per MONDO

Also identified as

• DOID 0080537 per MONDO
• OMIM 617013 per MONDO
• Orphanet 521406 per MONDO
• SCTID 768554008 per MONDO
• UMLS C4310765 per MONDO