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Schöpf–Schulz–Passarge syndrome

SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy
MedicalCondition developmental_defect_during_embryogenesis Q7433355
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Schöpf–Schulz–Passarge syndrome

Summary

Schöpf–Schulz–Passarge syndrome is a developmental defect during embryogenesis[1]. It draws 6 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2]

Key Facts

  • Schöpf–Schulz–Passarge syndrome's instance of is recorded as developmental defect during embryogenesis[3].
  • Schöpf–Schulz–Passarge syndrome's instance of is recorded as rare disease[4].
  • Schöpf–Schulz–Passarge syndrome's instance of is recorded as class of disease[5].
  • Schöpf–Schulz–Passarge syndrome's subclass of is recorded as nonepidermolytic palmoplantar keratoderma[6].
  • Schöpf–Schulz–Passarge syndrome's subclass of is recorded as autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature[7].
  • Schöpf–Schulz–Passarge syndrome's subclass of is recorded as malformation syndrome with odontal and/or periodontal component[8].
  • Schöpf–Schulz–Passarge syndrome's subclass of is recorded as polymalformative genetic syndrome with increased risk of developing cancer[9].
  • Schöpf–Schulz–Passarge syndrome's subclass of is recorded as autosomal dominant disease[10].
  • Schöpf–Schulz–Passarge syndrome's subclass of is recorded as ectodermal dysplasia[11].
  • Schöpf–Schulz–Passarge syndrome's MeSH descriptor ID is recorded as C565607[12].
  • Schöpf–Schulz–Passarge syndrome's OMIM ID is recorded as 224750[13].
  • Schöpf–Schulz–Passarge syndrome's ICD-10 ID is recorded as Q82.8[14].
  • Schöpf–Schulz–Passarge syndrome's KEGG ID is recorded as H00781[15].
  • Schöpf–Schulz–Passarge syndrome's Disease Ontology ID is recorded as DOID:0111647[16].
  • Schöpf–Schulz–Passarge syndrome's Orphanet ID is recorded as 50944[17].
  • Schöpf–Schulz–Passarge syndrome's ICD-9-CM is recorded as 758.89[18].
  • Schöpf–Schulz–Passarge syndrome's health specialty is recorded as medical genetics[19].
  • Schöpf–Schulz–Passarge syndrome's genetic association is recorded as WNT10A[20].
  • Schöpf–Schulz–Passarge syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_50944[21].
  • Schöpf–Schulz–Passarge syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111647[22].
  • Schöpf–Schulz–Passarge syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111647[23].
  • Schöpf–Schulz–Passarge syndrome's UMLS CUI is recorded as C1857069[24].
  • Schöpf–Schulz–Passarge syndrome's ICD-10-CM is recorded as Q82.8[25].
  • Schöpf–Schulz–Passarge syndrome's Mondo ID is recorded as MONDO_0009145[26].
  • Schöpf–Schulz–Passarge syndrome's Microsoft Academic ID is recorded as 2779686507[27].

Why It Matters

Schöpf–Schulz–Passarge syndrome draws 6 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2]

References

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

Direct Wikidata claims

  1. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [11] ↑ . Disease Ontology. Retrieved . wikidata.org.
  10. [12] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [13] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . Disease Ontology. Retrieved . wikidata.org.
  15. [17] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  16. [18] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . Disease Ontology. Retrieved . wikidata.org.
  21. [23] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  22. [24] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  23. [25] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.

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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). Schöpf–Schulz–Passarge syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/sch-pf-schulz-passarge-syndrome
MLA “Schöpf–Schulz–Passarge syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/sch-pf-schulz-passarge-syndrome.
BibTeX @misc{4ortxyz_sch-pf-schulz-passarge-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Schöpf–Schulz–Passarge syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/sch-pf-schulz-passarge-syndrome}, note = {Accessed: 2026-05-03}}
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