UMLS Hierarchy Tracer (Ancestors & Descendants)

Enter a Concept ID (CUI) to view its parent and child hierarchies. Select a preferred language for display names; **English will be used as a fallback**.

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

Target Concept: Hallermann Syndrome (C0018522)

Ancestor Paths (Parents/Root)

Ancestor Path 1 (Root Source: LIMIT)

  1. ... MAX DEPTH REACHED ... CUI: LIMIT / Source: LIMIT
  2. CUI: - / Source: MSH
  3. CUI: - / Source: MSH
  4. MeSH Descriptors CUI: C1256739 / Source: MSH
  5. Topical Descriptor CUI: C1256741 / Source: MSH
  6. Diseases (MeSH Category) CUI: C0012674 / Source: MSH
  7. Musculoskeletal Diseases CUI: C0026857 / Source: MSH
  8. Bone Diseases CUI: C0005940 / Source: MSH
  9. Bone Diseases, Developmental CUI: C0005941 / Source: MSH
  10. Dysostoses CUI: C0013393 / Source: MSH
  11. Craniofacial Dysostosis CUI: C0010273 / Source: MSH
  12. Hallermann Syndrome (START) CUI: C0018522 / 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. Musculoskeletal Diseases CUI: C0026857 / Source: MSH
  7. Musculoskeletal Abnormalities CUI: C0151491 / Source: MSH
  8. Craniofacial Abnormalities CUI: C0376634 / Source: MSH
  9. Craniofacial Dysostosis CUI: C0010273 / Source: MSH
  10. Hallermann Syndrome (START) CUI: C0018522 / Source: MSH

Ancestor Path 3 (Root Source: LIMIT)

  1. ... MAX DEPTH REACHED ... CUI: LIMIT / Source: LIMIT
  2. CUI: - / Source: MSH
  3. CUI: - / Source: MSH
  4. MeSH Descriptors CUI: C1256739 / Source: MSH
  5. Topical Descriptor CUI: C1256741 / Source: MSH
  6. Diseases (MeSH Category) CUI: C0012674 / Source: MSH
  7. Congenital, Hereditary, and Neonatal Diseases and Abnormalities CUI: C0027612 / Source: MSH
  8. Congenital Abnormalities CUI: C0000768 / Source: MSH
  9. Musculoskeletal Abnormalities CUI: C0151491 / Source: MSH
  10. Craniofacial Abnormalities CUI: C0376634 / Source: MSH
  11. Craniofacial Dysostosis CUI: C0010273 / Source: MSH
  12. Hallermann Syndrome (START) CUI: C0018522 / 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. Hallermann Syndrome (START) CUI: C0018522 / Source: MSH

Unique Ancestor Paths Found: 3 | Unique Descendant Paths Found: 1 | Max Depth: 10 levels.