cold-induced sweating syndrome

autosomal dominant disease characterized by problems with regulating body temperature and other abnormalities affecting many parts of the body; it has material basis in mutations in the CRLF1 gene
MedicalCondition rare_disease Q3961672
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cold-induced sweating syndrome

Summary

cold-induced sweating syndrome is a rare disease[1].

Key Facts

  • cold-induced sweating syndrome's instance of is recorded as rare disease[2].
  • cold-induced sweating syndrome's instance of is recorded as class of disease[3].
  • cold-induced sweating syndrome is a type of cold-induced sweating syndrome-hyperthermia spectrum[4].
  • cold-induced sweating syndrome is a type of autosomal dominant hereditary sensory and autonomic neuropathy[5].
  • cold-induced sweating syndrome is a type of syndrome[6].
  • cold-induced sweating syndrome is a type of autosomal recessive disease[7].
  • cold-induced sweating syndrome's NCI Thesaurus ID is recorded as C173147[8].
  • cold-induced sweating syndrome's health specialty is recorded as medical genetics[9].
  • cold-induced sweating syndrome's genetic association is recorded as KLHL7[10].
  • cold-induced sweating syndrome's genetic association is recorded as CRLF1[11].
  • cold-induced sweating syndrome's genetic association is recorded as CLCF1[12].
  • cold-induced sweating syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060294[13].
  • cold-induced sweating syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060294[14].
  • cold-induced sweating syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_157820[15].
  • cold-induced sweating syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].

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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] . Disease Ontology. Retrieved . wikidata.org.
  6. [7] . Disease Ontology. Retrieved . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa. wikidata.org.
  10. [11] . Cold-induced sweating syndrome is caused by mutations in the CRLF1 gene. wikidata.org.
  11. [12] . Inactivation of cardiotrophin-like cytokine, a second ligand for ciliary neurotrophic factor receptor, leads to cold-induced sweating syndrome in a patient. wikidata.org.
  12. [13] . Disease Ontology. Retrieved . wikidata.org.
  13. [14] . Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.

Class ancestry

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

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). cold-induced sweating syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/cold-induced-sweating-syndrome
MLA “cold-induced sweating syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cold-induced-sweating-syndrome.
BibTeX @misc{4ortxyz_cold-induced-sweating-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cold-induced sweating syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/cold-induced-sweating-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cold-induced sweating syndrome — https://4ort.xyz/entity/cold-induced-sweating-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/cold-induced-sweating-syndrome · Last refreshed:

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. 17w ago · Pi bot bot · 2026-05-22 view diff on Wikidata ↗
    Kegg id H00935
    Umls cui C1832409
    Imported from
    Instance of rare disease, class of disease
    + 15 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Add commons sitelink based on QID on Commons"
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