UMLS Hierarchy Tracer (Ancestors & Descendants)

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

Target Concept: Ellis-Van Creveld Syndrome (C0013903)

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. Ectodermal Dysplasia CUI: C0013575 / Source: MSH
  10. Ellis-Van Creveld Syndrome (START) CUI: C0013903 / 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. Skin and Connective Tissue Diseases CUI: C0175166 / Source: MSH
  7. Skin Diseases CUI: C0037274 / Source: MSH
  8. Skin Abnormalities CUI: C0037268 / Source: MSH
  9. Ectodermal Dysplasia CUI: C0013575 / Source: MSH
  10. Ellis-Van Creveld Syndrome (START) CUI: C0013903 / 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. Congenital, Hereditary, and Neonatal Diseases and Abnormalities CUI: C0027612 / Source: MSH
  7. Congenital Abnormalities CUI: C0000768 / Source: MSH
  8. Skin Abnormalities CUI: C0037268 / Source: MSH
  9. Ectodermal Dysplasia CUI: C0013575 / Source: MSH
  10. Ellis-Van Creveld Syndrome (START) CUI: C0013903 / 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. Skin and Connective Tissue Diseases CUI: C0175166 / Source: MSH
  7. Skin Diseases CUI: C0037274 / Source: MSH
  8. Skin Diseases, Genetic CUI: C0037277 / Source: MSH
  9. Ectodermal Dysplasia CUI: C0013575 / Source: MSH
  10. Ellis-Van Creveld Syndrome (START) CUI: C0013903 / 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. Congenital, Hereditary, and Neonatal Diseases and Abnormalities CUI: C0027612 / Source: MSH
  7. Genetic Diseases, Inborn CUI: C0950123 / Source: MSH
  8. Skin Diseases, Genetic CUI: C0037277 / Source: MSH
  9. Ectodermal Dysplasia CUI: C0013575 / Source: MSH
  10. Ellis-Van Creveld Syndrome (START) CUI: C0013903 / 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. Musculoskeletal Diseases CUI: C0026857 / Source: MSH
  7. Bone Diseases CUI: C0005940 / Source: MSH
  8. Bone Diseases, Developmental CUI: C0005941 / Source: MSH
  9. Osteochondrodysplasias CUI: C0029422 / Source: MSH
  10. Ellis-Van Creveld Syndrome (START) CUI: C0013903 / 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. Osteochondrodysplasias CUI: C0029422 / Source: MSH
  9. Ellis-Van Creveld Syndrome (START) CUI: C0013903 / 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. Ellis-Van Creveld Syndrome (START) CUI: C0013903 / Source: MSH

Unique Ancestor Paths Found: 7 | Unique Descendant Paths Found: 1 | Max Depth: 10 levels.