UMLS Hierarchy Tracer (Ancestors & Descendants)

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Displaying names in **English (ENG)** (with English fallback).

Target Concept: Hallervorden-Spatz Syndrome (C0018523)

Ancestor Paths (Parents/Root)

Ancestor Path 1 (Root Source: MSH)

  1. CUI: - / Source: MSH
  2. CUI: - / Source: MSH
  3. MeSH Descriptors CUI: C1256739 / Source: MSH
  4. Topical Descriptor CUI: C1256741 / Source: MSH
  5. Diseases (MeSH Category) CUI: C0012674 / Source: MSH
  6. Nervous System Diseases CUI: C0027765 / Source: MSH
  7. Central Nervous System Diseases CUI: C0007682 / Source: MSH
  8. Brain Diseases CUI: C0006111 / Source: MSH
  9. Basal Ganglia Diseases CUI: C0004782 / Source: MSH
  10. Hallervorden-Spatz Syndrome (START) CUI: C0018523 / Source: MSH

Ancestor Path 2 (Root Source: MSH)

  1. CUI: - / Source: MSH
  2. CUI: - / Source: MSH
  3. MeSH Descriptors CUI: C1256739 / Source: MSH
  4. Topical Descriptor CUI: C1256741 / Source: MSH
  5. Diseases (MeSH Category) CUI: C0012674 / Source: MSH
  6. Nervous System Diseases CUI: C0027765 / Source: MSH
  7. Central Nervous System Diseases CUI: C0007682 / Source: MSH
  8. Movement Disorders CUI: C0026650 / Source: MSH
  9. Hallervorden-Spatz Syndrome (START) CUI: C0018523 / Source: MSH

Ancestor Path 3 (Root Source: MSH)

  1. CUI: - / Source: MSH
  2. CUI: - / Source: MSH
  3. MeSH Descriptors CUI: C1256739 / Source: MSH
  4. Topical Descriptor CUI: C1256741 / Source: MSH
  5. Diseases (MeSH Category) CUI: C0012674 / Source: MSH
  6. Nervous System Diseases CUI: C0027765 / Source: MSH
  7. Central Nervous System Diseases CUI: C0007682 / Source: MSH
  8. Brain Diseases CUI: C0006111 / Source: MSH
  9. Neuroaxonal Dystrophies CUI: C0338473 / Source: MSH
  10. Hallervorden-Spatz Syndrome (START) CUI: C0018523 / Source: MSH

Ancestor Path 4 (Root Source: MSH)

  1. CUI: - / Source: MSH
  2. CUI: - / Source: MSH
  3. MeSH Descriptors CUI: C1256739 / Source: MSH
  4. Topical Descriptor CUI: C1256741 / Source: MSH
  5. Diseases (MeSH Category) CUI: C0012674 / Source: MSH
  6. Nervous System Diseases CUI: C0027765 / Source: MSH
  7. Neurodegenerative Diseases CUI: C0524851 / Source: MSH
  8. Heredodegenerative Disorders, Nervous System CUI: C0751870 / Source: MSH
  9. Hallervorden-Spatz Syndrome (START) CUI: C0018523 / Source: MSH

Ancestor Path 5 (Root Source: MSH)

  1. CUI: - / Source: MSH
  2. CUI: - / Source: MSH
  3. MeSH Descriptors CUI: C1256739 / Source: MSH
  4. Topical Descriptor CUI: C1256741 / Source: MSH
  5. Diseases (MeSH Category) CUI: C0012674 / Source: MSH
  6. Congenital, Hereditary, and Neonatal Diseases and Abnormalities CUI: C0027612 / Source: MSH
  7. Genetic Diseases, Inborn CUI: C0950123 / Source: MSH
  8. Heredodegenerative Disorders, Nervous System CUI: C0751870 / Source: MSH
  9. Hallervorden-Spatz Syndrome (START) CUI: C0018523 / Source: MSH

Descendant Paths (Children/Leaves)

This concept appears to be a Leaf node in the available hierarchies (showing only the starting concept).

Descendant Path 1 (Top Source: MSH)

  1. Hallervorden-Spatz Syndrome (START) CUI: C0018523 / Source: MSH

Unique Ancestor Paths Found: 5 | Unique Descendant Paths Found: 1 | Max Depth: 10 levels.