microcephalic primordial dwarfism, Alazami type

human disease
MedicalCondition developmental_defect_during_embryogenesis Q55784484
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microcephalic primordial dwarfism, Alazami type

Summary

microcephalic primordial dwarfism, Alazami type is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]

Key Facts

  • microcephalic primordial dwarfism, Alazami type's instance of is recorded as developmental defect during embryogenesis[3].
  • microcephalic primordial dwarfism, Alazami type's instance of is recorded as rare disease[4].
  • microcephalic primordial dwarfism, Alazami type's instance of is recorded as class of disease[5].
  • microcephalic primordial dwarfism, Alazami type is a type of microcephalic primordial dwarfism[6].
  • microcephalic primordial dwarfism, Alazami type's genetic association is recorded as LARP7[7].
  • microcephalic primordial dwarfism, Alazami type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_319671[8].

Why It Matters

microcephalic primordial dwarfism, Alazami type is known by 5 alternative names across languages and contexts.[2]

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APA 4ort.xyz Knowledge Graph. (2026). microcephalic primordial dwarfism, Alazami type. Retrieved May 3, 2026, from https://4ort.xyz/entity/microcephalic-primordial-dwarfism-alazami-type
MLA “microcephalic primordial dwarfism, Alazami type.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/microcephalic-primordial-dwarfism-alazami-type.
BibTeX @misc{4ortxyz_microcephalic-primordial-dwarfism-alazami-type_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{microcephalic primordial dwarfism, Alazami type}}, year = {2026}, url = {https://4ort.xyz/entity/microcephalic-primordial-dwarfism-alazami-type}, 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. 11w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0014031
    Genetic association LARP7
    Kegg id H02233
    Orphanet id 319671
    + 9 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
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