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MDP syndrome

human disease
Class type of: Hearing loss with craniofacial syndromes, progeroid syndrome, syndromic genetic deafness Q17120696

Facts

5 properties
Instance of
rare disease, class of disease[6]
Subclass of
Hearing loss with craniofacial syndromes, progeroid syndrome, syndromic genetic deafness, developmental defect during embryogenesis, head and neck disease[7]
Age of onset
childhood onset[10]
Genetic association
POLD1[9]
Prevalence
+0.000001[8]
🏷️ Also known as
en Mandibular hypoplasia-hearing loss-progeroid syndrome en MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME en MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL en MDPL en MDP syndrome ar متلازمة MDP fr syndrome d'hypoplasie mandibulaire-surdité-aspect progéroïde
🔖 Identifiers · 10
Exact match
www.orpha.net
GARD rare disease ID
10989
ICD-10-CM
E34.8
Microsoft Academic ID (discontinued)
2781123483, 2911031850
Mondo ID
MONDO_0014157
OMIM ID
615381
Orphanet ID
363649
Raras disease ID
D363649
UMLS CUI
C3715192
UniProt disease ID
DI-03863

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Summary

MDP syndrome is a rare disease[1]. It is a type of Hearing loss with craniofacial syndromes[2], progeroid syndrome[3], syndromic genetic deafness[4], and developmental defect during embryogenesis[5].

References

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

Direct Wikidata claims

  1. [6] ↑ . wikidata.org.
  2. [2] ↑ . wikidata.org.
  3. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] ↑ . Retrieved . wikidata.org.
  8. [9] ↑ . UniProt. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  9. [10] ↑ . Retrieved . 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). MDP syndrome. Retrieved November 9, 2026, from https://4ort.xyz/entity/mdp-syndrome
MLA “MDP syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 9 Nov. 2026, https://4ort.xyz/entity/mdp-syndrome.
BibTeX @misc{4ortxyz_mdp-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{MDP syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/mdp-syndrome}, note = {Accessed: 2026-11-09}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): MDP syndrome — https://4ort.xyz/entity/mdp-syndrome (retrieved 2026-11-09)

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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. 19d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Prevalence → 0.000001
    Age of onset → childhood onset
    Raras disease ID → D363649
    "Changed labels, descriptions, aliases and claims: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo ID → MONDO_0014157
    Genetic association → POLD1
    GARD rare disease ID → 10989
    Orphanet ID → 363649
    + 10 other properties edited (see Wikidata diff for full list)
    "Changed the item: QuickStatements 3.0 batch #39742: subclass of disease, not instance"
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