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: Hippel Lindau Disease (C0019562)

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. Cardiovascular Diseases CUI: C0007222 / Source: MSH
  7. Vascular Diseases CUI: C0042373 / Source: MSH
  8. Angiomatosis CUI: C0002992 / Source: MSH
  9. Hippel Lindau Disease (START) CUI: C0019562 / Source: MSH

Ancestor Path 2 (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. Abnormalities, Multiple CUI: C0000772 / Source: MSH
  10. Ectodermal Dysplasia CUI: C0013575 / Source: MSH
  11. Neurocutaneous Syndromes CUI: C0265316 / Source: MSH
  12. Hippel Lindau Disease (START) CUI: C0019562 / 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. Skin and Connective Tissue Diseases CUI: C0175166 / Source: MSH
  8. Skin Diseases CUI: C0037274 / Source: MSH
  9. Skin Abnormalities CUI: C0037268 / Source: MSH
  10. Ectodermal Dysplasia CUI: C0013575 / Source: MSH
  11. Neurocutaneous Syndromes CUI: C0265316 / Source: MSH
  12. Hippel Lindau Disease (START) CUI: C0019562 / Source: MSH

Ancestor Path 4 (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. Skin Abnormalities CUI: C0037268 / Source: MSH
  10. Ectodermal Dysplasia CUI: C0013575 / Source: MSH
  11. Neurocutaneous Syndromes CUI: C0265316 / Source: MSH
  12. Hippel Lindau Disease (START) CUI: C0019562 / Source: MSH

Ancestor Path 5 (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. Skin and Connective Tissue Diseases CUI: C0175166 / Source: MSH
  8. Skin Diseases CUI: C0037274 / Source: MSH
  9. Skin Diseases, Genetic CUI: C0037277 / Source: MSH
  10. Ectodermal Dysplasia CUI: C0013575 / Source: MSH
  11. Neurocutaneous Syndromes CUI: C0265316 / Source: MSH
  12. Hippel Lindau Disease (START) CUI: C0019562 / Source: MSH

Ancestor Path 6 (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. Genetic Diseases, Inborn CUI: C0950123 / Source: MSH
  9. Skin Diseases, Genetic CUI: C0037277 / Source: MSH
  10. Ectodermal Dysplasia CUI: C0013575 / Source: MSH
  11. Neurocutaneous Syndromes CUI: C0265316 / Source: MSH
  12. Hippel Lindau Disease (START) CUI: C0019562 / Source: MSH

Ancestor Path 7 (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. Neurocutaneous Syndromes CUI: C0265316 / Source: MSH
  8. Hippel Lindau Disease (START) CUI: C0019562 / Source: MSH

Ancestor Path 8 (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. Congenital Abnormalities CUI: C0000768 / Source: MSH
  8. Abnormalities, Multiple CUI: C0000772 / Source: MSH
  9. Ciliopathies CUI: C4277690 / Source: MSH
  10. Hippel Lindau Disease (START) CUI: C0019562 / Source: MSH

Ancestor Path 9 (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. Ciliopathies CUI: C4277690 / Source: MSH
  9. Hippel Lindau Disease (START) CUI: C0019562 / 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. Hippel Lindau Disease (START) CUI: C0019562 / Source: MSH

Unique Ancestor Paths Found: 9 | Unique Descendant Paths Found: 1 | Max Depth: 10 levels.