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

Official abbreviation NBIA2B
Name neurodegeneration, with brain iron accumulation, type 2B (NBIA-2B)
OMIM ID 610217
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PLA2G6
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00080820 - PubMed: Trujillano 2017 unaffected heterozygous carrier parents - - - - - - - - NBIA2B Neurodegeneration with brain iron accumulation 2B (OMIM:610217) PLA2G6 PLA2G6 1 1 Daniel Trujillano
00472134 279055 - - M no ? (unknown) - - - - - NBIA2B Neurodegeneration, Iron accumulation in brain, Progressive cerebellar ataxia, Tremor, Bradykinesia, Dysmetria, Axial hypotonia, Dysarthria, Gait ataxia, Rigidity, Akinesia, Cerebellar atrophy, Hyperreflexia PLA2G6 PLA2G6 2 1 Andreas Laner
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