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Basal Ganglia Diseases - C0004782 L0004782 S0017860 A0029264 M0002198 MeSH MH D001480 → |
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Basal Ganglia Diseases - C0004782 L0004782 S0017860 A0029264 M0002198 MeSH MH D001480 → |
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Basal Ganglia Disorder - C0004782 L1403726 S1674537 A1636359 M0002198 MeSH PM D001480 → |
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Basal Ganglia Disorder - C0004782 L1403726 S1674537 A1636359 M0002198 MeSH PM D001480 → |
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Basal Ganglia Disorders - C0004782 L1403726 S1674538 A1636360 M0002198 MeSH EN D001480 → |
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Basal Ganglia Disorders - C0004782 L1403726 S1674538 A1636360 M0002198 MeSH EN D001480 → |
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Basal Lamina (MeSH) - C0085872 L0004783 S0017862 A7756456 M0002215 MeSH PEP D001485 → |
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Basal Laminas (MeSH) - C0085872 L0004783 S0017863 A0029266 M0002215 MeSH PM D001485 → |
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Basal Nuclei - C0004781 L0004787 S0017867 A0029271 M0002196 MeSH EP D001479 → |
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Basal Nuclei - C0004781 L0004787 S0017867 A0029271 M0002196 MeSH EP D001479 → |
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