UMLS Hierarchy Tracer (Ancestors & Descendants)

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

Target Concept: Hyper-Immunoglobulin E Syndrome, Autosomal Dominant (C2936739)

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. Immune System Diseases CUI: C0021053 / Source: MSH
  7. Immunologic Deficiency Syndromes CUI: C0021051 / Source: MSH
  8. Phagocyte Bactericidal Dysfunction CUI: C0031306 / Source: MSH
  9. Hyper-Immunoglobulin E Syndrome, Autosomal Dominant (START) CUI: C2936739 / 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. Hemic and Lymphatic Diseases CUI: C0851353 / Source: MSH
  7. Hematologic Diseases CUI: C0018939 / Source: MSH
  8. Leukocyte Disorders CUI: C0023510 / Source: MSH
  9. Phagocyte Bactericidal Dysfunction CUI: C0031306 / Source: MSH
  10. Hyper-Immunoglobulin E Syndrome, Autosomal Dominant (START) CUI: C2936739 / 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. Immune System Diseases CUI: C0021053 / Source: MSH
  7. Immunologic Deficiency Syndromes CUI: C0021051 / Source: MSH
  8. Primary Immunodeficiency Diseases CUI: C0398686 / Source: MSH
  9. Hyper-Immunoglobulin E Syndrome, Autosomal Dominant (START) CUI: C2936739 / 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. Congenital, Hereditary, and Neonatal Diseases and Abnormalities CUI: C0027612 / Source: MSH
  7. Genetic Diseases, Inborn CUI: C0950123 / Source: MSH
  8. Primary Immunodeficiency Diseases CUI: C0398686 / Source: MSH
  9. Hyper-Immunoglobulin E Syndrome, Autosomal Dominant (START) CUI: C2936739 / 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. Hyper-Immunoglobulin E Syndrome, Autosomal Dominant (START) CUI: C2936739 / Source: MSH

Unique Ancestor Paths Found: 4 | Unique Descendant Paths Found: 1 | Max Depth: 10 levels.