UMLS Hierarchy Tracer (Ancestors & Descendants)

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

Target Concept: Oculocerebrorenal Syndrome (C0028860)

Path Limit Reached (500 paths):

Hierarchy traversal was stopped for the capped direction(s). **All first-level children/parents are now guaranteed to be included,** but paths beyond Level 1 may be incomplete. (Ancestor Raw Count: **515** | Descendant Raw Count: **0**)

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. 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. Oculocerebrorenal Syndrome (START) CUI: C0028860 / Source: MSH

Ancestor Path 2 (Root Source: LIMIT)

  1. ... MAX DEPTH REACHED ... CUI: LIMIT / Source: LIMIT
  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. Urogenital Diseases CUI: C0080276 / Source: MSH
  7. Female Urogenital Diseases and Pregnancy Complications CUI: C1720765 / Source: MSH
  8. Female Urogenital Diseases CUI: C1720887 / Source: MSH
  9. Urologic Diseases CUI: C0042075 / Source: MSH
  10. Kidney Diseases CUI: C0022658 / Source: MSH
  11. Renal Tubular Transport, Inborn Errors CUI: C0035091 / Source: MSH
  12. Oculocerebrorenal Syndrome (START) CUI: C0028860 / 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. Urogenital Diseases CUI: C0080276 / Source: MSH
  8. Male Urogenital Diseases CUI: C1720894 / Source: MSH
  9. Urologic Diseases CUI: C0042075 / Source: MSH
  10. Kidney Diseases CUI: C0022658 / Source: MSH
  11. Renal Tubular Transport, Inborn Errors CUI: C0035091 / Source: MSH
  12. Oculocerebrorenal Syndrome (START) CUI: C0028860 / 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. Urogenital Diseases CUI: C0080276 / Source: MSH
  7. Urologic Diseases CUI: C0042075 / Source: MSH
  8. Kidney Diseases CUI: C0022658 / Source: MSH
  9. Renal Tubular Transport, Inborn Errors CUI: C0035091 / Source: MSH
  10. Oculocerebrorenal Syndrome (START) CUI: C0028860 / 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. Nutritional and Metabolic Diseases CUI: C0028715 / Source: MSH
  7. Metabolic Diseases CUI: C0025517 / Source: MSH
  8. Metabolism, Inborn Errors CUI: C0025521 / Source: MSH
  9. Renal Tubular Transport, Inborn Errors CUI: C0035091 / Source: MSH
  10. Oculocerebrorenal Syndrome (START) CUI: C0028860 / Source: MSH

Ancestor Path 6 (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. Metabolism, Inborn Errors CUI: C0025521 / Source: MSH
  9. Renal Tubular Transport, Inborn Errors CUI: C0035091 / Source: MSH
  10. Oculocerebrorenal Syndrome (START) CUI: C0028860 / 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. Congenital, Hereditary, and Neonatal Diseases and Abnormalities CUI: C0027612 / Source: MSH
  7. Genetic Diseases, Inborn CUI: C0950123 / Source: MSH
  8. Renal Tubular Transport, Inborn Errors CUI: C0035091 / Source: MSH
  9. Oculocerebrorenal Syndrome (START) CUI: C0028860 / Source: MSH

Ancestor Path 8 (Root Source: MSH)

  1. Renal Tubular Transport, Inborn Errors CUI: C0035091 / Source: MSH
  2. Oculocerebrorenal Syndrome (START) CUI: C0028860 / Source: MSH

Ancestor Path 9 (Root Source: MSH)

  1. Amino Acid Transport Disorders, Inborn CUI: C0751746 / Source: MSH
  2. Oculocerebrorenal Syndrome (START) CUI: C0028860 / Source: MSH

Ancestor Path 10 (Root Source: MSH)

  1. Brain Diseases, Metabolic, Inborn CUI: C0752109 / Source: MSH
  2. Oculocerebrorenal Syndrome (START) CUI: C0028860 / Source: MSH

Ancestor Path 11 (Root Source: MSH)

  1. Genetic Diseases, Inborn CUI: C0950123 / Source: MSH
  2. Oculocerebrorenal Syndrome (START) CUI: C0028860 / Source: MSH

Ancestor Path 12 (Root Source: MSH)

  1. Genetic Diseases, X-Linked CUI: C1138434 / Source: MSH
  2. Oculocerebrorenal Syndrome (START) CUI: C0028860 / 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. Oculocerebrorenal Syndrome (START) CUI: C0028860 / Source: MSH

Unique Ancestor Paths Found: 12 | Unique Descendant Paths Found: 1 | Max Depth: 10 levels.