hereditary central diabetes insipidus

subtype of central diabetes insipidus (CDI, see this term) characterized by polyuria and polydipsia due to a genetically inherited decrease in vasopressin (AVP) production
MedicalCondition class_of_disease Q138495840
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hereditary central diabetes insipidus

Summary

hereditary central diabetes insipidus is a class of disease[1].

Key Facts

  • hereditary central diabetes insipidus's image is recorded as Arginine vasopressin3d.png[2].
  • hereditary central diabetes insipidus's instance of is recorded as class of disease[3].
  • hereditary central diabetes insipidus's instance of is recorded as rare disease[4].
  • hereditary central diabetes insipidus's subclass of is recorded as central diabetes insipidus[5].
  • hereditary central diabetes insipidus's subclass of is recorded as endocrine system disease[6].
  • hereditary central diabetes insipidus's subclass of is recorded as genetic disease[7].
  • hereditary central diabetes insipidus's subclass of is recorded as pituitary deficiency[8].
  • hereditary central diabetes insipidus's subclass of is recorded as hypopituitarism[9].
  • hereditary central diabetes insipidus's part of is recorded as central diabetes insipidus[10].
  • hereditary central diabetes insipidus's opposite of is recorded as acquired central diabetes insipidus[11].
  • hereditary central diabetes insipidus's OMIM ID is recorded as 125700[12].
  • hereditary central diabetes insipidus's OMIM ID is recorded as 304900[13].
  • hereditary central diabetes insipidus's ICD-9 ID is recorded as 253.5[14].
  • hereditary central diabetes insipidus's ICD-10 ID is recorded as E23.2[15].
  • hereditary central diabetes insipidus's ICPC 2 ID is recorded as T99[16].
  • hereditary central diabetes insipidus's afflicts is recorded as Homo sapiens[17].
  • hereditary central diabetes insipidus's afflicts is recorded as mammal[18].
  • hereditary central diabetes insipidus's Disease Ontology ID is recorded as DOID:12388[19].
  • hereditary central diabetes insipidus's symptoms and signs is recorded as polyuria[20].
  • hereditary central diabetes insipidus's symptoms and signs is recorded as polydipsia[21].
  • hereditary central diabetes insipidus's symptoms and signs is recorded as nocturia[22].
  • hereditary central diabetes insipidus's symptoms and signs is recorded as hyposthenuria[23].
  • hereditary central diabetes insipidus's has cause is recorded as mutation[24].
  • hereditary central diabetes insipidus's medical examination is recorded as genetic testing[25].
  • hereditary central diabetes insipidus's possible treatment is recorded as medication[26].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . wikidata.org.
  11. [12] . wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . wikidata.org.
  21. [22] . wikidata.org.
  22. [23] . wikidata.org.
  23. [24] . wikidata.org.
  24. [25] . wikidata.org.
  25. [26] . nhs.uk. nhs.uk. Provenance: wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). hereditary central diabetes insipidus. Retrieved May 3, 2026, from https://4ort.xyz/entity/hereditary-central-diabetes-insipidus
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BibTeX @misc{4ortxyz_hereditary-central-diabetes-insipidus_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hereditary central diabetes insipidus}}, year = {2026}, url = {https://4ort.xyz/entity/hereditary-central-diabetes-insipidus}, note = {Accessed: 2026-05-03}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 6w ago · Tunyk · 2026-05-05 view diff on Wikidata ↗
    Icpc 2 id T99
    Disease ontology id DOID:12388
    Icd-9 id 253.5
    Malacards id hereditary_arginine_vasopressin_deficiency
    + 35 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-create:2||1 */ [[Property:P279]]: [[Q179630]]"
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