Phenotypes for disease #05698 (HMNDYT2 (hypermanganesemia with dystonia, type 2 (HMNDYT2)), OMIM:617013)

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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000223347 4 limbs spastic cerebral palsy,Neuroferritinopathy Hypermanganesemia increased muscle tone,microcephaly,global developmental delay,profound physical disability. Familial, autosomal recessive 01y 05y 00y08m increased muscle tone Adel ZEeglam 00295870
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