patterned macular dystrophy

macular degeneration characterized by abnormal accumulation of lipofuscin in the retinal pigment epithelium in a distinct pattern, patterns include; reticular ('fishnet-like'), macroreticular ('spider-shaped'), and butterfly-shaped

Facts

6 properties
Instance of
rare disease, class of disease[3]
Age of onset
adult onset[8]
Genetic association
PRPH2, CTNNA1, OTX2[5][6][7]
On focus list of Wikimedia project
WikiProject Medicine[9]
Prevalence
+0.000001[4]
🏷️ Also known as
en patterned dystrophy of retinal pigment epithelium en patterned macular dystrophy fr dystrophie tachetée du pôle postérieur
🔖 Identifiers · 9
Disease Ontology ID
DOID:0060863
GARD rare disease ID
9821
ICD-10-CM
H35.5
KEGG ID
H01890
Orphanet ID
99001
PatientsLikeMe condition ID
pattern-macular-dystrophy
Raras disease ID
D99001
UMLS CUI
C1868569

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Summary

patterned macular dystrophy is a rare disease[1]. It is a type of macular degeneration[2].

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APA 4ort.xyz Knowledge Graph. (2026). patterned macular dystrophy. Retrieved October 24, 2026, from https://4ort.xyz/entity/patterned-macular-dystrophy
MLA “patterned macular dystrophy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 24 Oct. 2026, https://4ort.xyz/entity/patterned-macular-dystrophy.
BibTeX @misc{4ortxyz_patterned-macular-dystrophy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{patterned macular dystrophy}}, year = {2026}, url = {https://4ort.xyz/entity/patterned-macular-dystrophy}, note = {Accessed: 2026-10-24}}
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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 ↗
    Instance of → rare disease, class of disease
    UMLS CUI → C1868569
    Genetic association → PRPH2, CTNNA1, OTX2
    KEGG ID → H01890
    + 12 other properties edited (see Wikidata diff for full list)
    "Changed labels, descriptions, aliases and claims: QuickStatements 3.0 batch #61469: Raras.org data import"
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