UMLS Hierarchy Tracer (Ancestors & Descendants)

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

Target Concept: Benign Monoclonal Gammopathy (C0026470)

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. Hemic and Lymphatic Diseases CUI: C0851353 / Source: MSH
  7. Hematologic Diseases CUI: C0018939 / Source: MSH
  8. Blood Protein Disorders CUI: C0005830 / Source: MSH
  9. Hypergammaglobulinemia CUI: C0020455 / Source: MSH
  10. Benign Monoclonal Gammopathy (START) CUI: C0026470 / 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. Immune System Diseases CUI: C0021053 / Source: MSH
  7. Immunoproliferative Disorders CUI: C0021070 / Source: MSH
  8. Hypergammaglobulinemia CUI: C0020455 / Source: MSH
  9. Benign Monoclonal Gammopathy (START) CUI: C0026470 / 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. Pathological Conditions, Signs and Symptoms CUI: C0039058 / Source: MSH
  7. Signs and Symptoms CUI: C0037088 / Source: MSH
  8. Hypergammaglobulinemia CUI: C0020455 / Source: MSH
  9. Benign Monoclonal Gammopathy (START) CUI: C0026470 / 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. Hemic and Lymphatic Diseases CUI: C0851353 / Source: MSH
  7. Hematologic Diseases CUI: C0018939 / Source: MSH
  8. Blood Protein Disorders CUI: C0005830 / Source: MSH
  9. Paraproteinemias CUI: C0030489 / Source: MSH
  10. Benign Monoclonal Gammopathy (START) CUI: C0026470 / 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. Immune System Diseases CUI: C0021053 / Source: MSH
  7. Immunoproliferative Disorders CUI: C0021070 / Source: MSH
  8. Paraproteinemias CUI: C0030489 / Source: MSH
  9. Benign Monoclonal Gammopathy (START) CUI: C0026470 / Source: MSH

Descendant Paths (Children/Leaves)

Descendant Path 1 (Top Source: MSH)

  1. Benign Monoclonal Gammopathy (START) CUI: C0026470 / Source: MSH
  2. Schnitzler Syndrome CUI: C0524988 / Source: MSH

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