Also known as Hallervorden-Spatz disease, Hallervorden-Spatz syndrome, brain Iron Accumulation type I syndrome, neurodegeneration with brain iron accumulation 1, NBIA1, pigmentary pallidal degeneration (disorder)
via Wikidata · CC0
neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13
via Wikidata sitelinks · CC0
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).