UMLS Hierarchy Tracer (Ancestors & Descendants)

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

Target Concept: Renal Tubular Transport, Inborn Errors (C0035091)

Ancestor Paths (Parents/Root)

Ancestor Path 1 (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. Female Urogenital Diseases and Pregnancy Complications CUI: C1720765 / Source: MSH
  9. Female Urogenital Diseases CUI: C1720887 / Source: MSH
  10. Urologic Diseases CUI: C0042075 / Source: MSH
  11. Kidney Diseases CUI: C0022658 / Source: MSH
  12. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / 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. Urogenital Diseases CUI: C0080276 / Source: MSH
  7. Male Urogenital Diseases CUI: C1720894 / Source: MSH
  8. Urologic Diseases CUI: C0042075 / Source: MSH
  9. Kidney Diseases CUI: C0022658 / Source: MSH
  10. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / 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. 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 (START) CUI: C0035091 / 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. 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 (START) CUI: C0035091 / 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. Metabolism, Inborn Errors CUI: C0025521 / Source: MSH
  9. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / 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. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH

Descendant Paths (Children/Leaves)

Descendant Path 1 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Acidosis, Renal Tubular CUI: C0001126 / Source: MSH

Descendant Path 2 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Fanconi Syndrome CUI: C0015624 / Source: MSH

Descendant Path 3 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Glycosuria, Renal CUI: C3245525 / Source: MSH

Descendant Path 4 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Hypophosphatemia, Familial CUI: C0020631 / Source: MSH
  3. Familial Hypophosphatemic Rickets CUI: C3536983 / Source: MSH

Descendant Path 5 (Top Source: MSH)

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

Descendant Path 6 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Pseudohypoaldosteronism CUI: C0033805 / Source: MSH

Descendant Path 7 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Gitelman Syndrome CUI: C0268450 / Source: MSH

Descendant Path 8 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Renal Aminoacidurias CUI: C0002534 / Source: MSH
  3. Cystinuria CUI: C0010691 / Source: MSH

Descendant Path 9 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Renal Aminoacidurias CUI: C0002534 / Source: MSH
  3. Hartnup Disease CUI: C0018609 / Source: MSH

Descendant Path 10 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Liddle Syndrome CUI: C0221043 / Source: MSH

Descendant Path 11 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Dent Disease CUI: C0878681 / Source: MSH

Descendant Path 12 (Top Source: MSH)

  1. Renal Tubular Transport, Inborn Errors (START) CUI: C0035091 / Source: MSH
  2. Bartter Syndrome CUI: C0004775 / Source: MSH

Unique Ancestor Paths Found: 6 | Unique Descendant Paths Found: 12 | Max Depth: 10 levels.