FRAXE intellectual disability

FRAXE is a form of nonsyndromic X-linked mental retardation (NS-XLMR) characterized by mild intellectual deficit. FRAXE is the most common form of NS-XLMR.
MedicalCondition hereditary_disorder Q21051307
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FRAXE intellectual disability

Summary

FRAXE intellectual disability is a hereditary disorder[1]. It is known by 12 alternative names across languages and contexts.[2]

Key Facts

  • FRAXE intellectual disability's instance of is recorded as hereditary disorder[3].
  • FRAXE intellectual disability's instance of is recorded as rare disease[4].
  • FRAXE intellectual disability's instance of is recorded as class of disease[5].
  • FRAXE intellectual disability is a type of non-syndromic X-linked intellectual disability[6].
  • FRAXE intellectual disability is a type of X-linked intellectual disability[7].
  • FRAXE intellectual disability's genetic association is recorded as Fragile Mental Retardation 2[8].
  • FRAXE intellectual disability's genetic association is recorded as AFF2[9].
  • FRAXE intellectual disability's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_100973[10].

Why It Matters

FRAXE intellectual disability is known by 12 alternative names across languages and contexts.[2]

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APA 4ort.xyz Knowledge Graph. (2026). FRAXE intellectual disability. Retrieved May 3, 2026, from https://4ort.xyz/entity/fraxe-intellectual-disability
MLA “FRAXE intellectual disability.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/fraxe-intellectual-disability.
BibTeX @misc{4ortxyz_fraxe-intellectual-disability_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{FRAXE intellectual disability}}, year = {2026}, url = {https://4ort.xyz/entity/fraxe-intellectual-disability}, 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. 10w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0010659
    Genetic association Fragile Mental Retardation 2, AFF2
    Gard rare disease id 2378
    Orphanet id 100973
    + 7 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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