has material basis in germline mutation in SLC30A10 hypermanganesemia with dystonia cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome https://www.malacards.org/card/hypermanganesemia_with_dystonia_1 ICD9:277.89 MESH:C548016 HMNDYT1 HMDPC GARD:0010706 OMIM:613280 MONDO:0013208 hypermanganesemia with dystonia, polycythemia, and cirrhosis SCTID:702377007 cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome DOID:0080536 hypermanganesemia with dystonia polycythemia and cirrhosis UMLS:C2750442 MEDGEN:412958 Orphanet:309854 disorder of manganese transport parkinsonian disorder hereditary neurological disease