Phenotypes for disease #00760 (NBIA2B (neurodegeneration, with brain iron accumulation, type 2B (NBIA-2B)), OMIM:610217)

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AscendingPhenotype ID     

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Individual ID     
0000060389 Neurodegeneration with brain iron accumulation 2B (OMIM:610217) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080820
0000356942 Neurodegeneration, Iron accumulation in brain, Progressive cerebellar ataxia, Tremor, Bradykinesia, Dysmetria, Axial hypotonia, Dysarthria, Gait ataxia, Rigidity, Akinesia, Cerebellar atrophy, Hyperreflexia - - Unknown 17y - - - - Andreas Laner 00472134
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