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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00295870 - - - M yes Libya white 06y - - - HMNDYT2 increased muscle tone,microcephaly,global developmental delay,profound physical disability. SLC39A14 SLC39A14 1 1 Adel ZEeglam
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