Perry syndrome
E1551036
UNEXPLORED
Perry syndrome is a rare, inherited neurodegenerative disorder characterized by parkinsonism, depression, weight loss, and respiratory failure, typically caused by mutations in the DCTN1 gene.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Perry syndrome canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T22693225 — resolving that mention is where its identity was fixed. The disambiguator weighed these candidate entities and picked the highlighted one (or “None”, minting a new entity). This is how homonymy is resolved: the same surface form can point to different entities.
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Perry syndrome Context triple: [TDP-43 proteinopathy, associatedWithDisease, Perry syndrome]
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A.
Kotov Syndrome
Kotov Syndrome is a chess-related psychological phenomenon where a player, after long and intense calculation, becomes mentally exhausted and suddenly makes a blunder or inferior move.
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B.
Bendii Syndrome
Bendii Syndrome is a rare degenerative neurological illness in the Star Trek universe that affects elderly Vulcans, causing emotional instability and loss of mental control.
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C.
Vrolik syndrome
Vrolik syndrome, also known as osteogenesis imperfecta type II, is a severe genetic disorder characterized by extremely fragile bones that fracture easily, often leading to perinatal lethality.
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D.
Florence syndrome
Florence syndrome is a psychosomatic condition in which individuals experience dizziness, rapid heartbeat, confusion, or even hallucinations when exposed to overwhelming art or beauty, particularly in culturally rich cities like Florence.
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E.
Joubbé
Joubbé is a locality in Lebanon that forms part of the pastoral territory served by the Maronite Catholic Eparchy of Joubbé, Sarba and Jounieh.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: Perry syndrome Target entity description: Perry syndrome is a rare, inherited neurodegenerative disorder characterized by parkinsonism, depression, weight loss, and respiratory failure, typically caused by mutations in the DCTN1 gene.
-
A.
Kotov Syndrome
Kotov Syndrome is a chess-related psychological phenomenon where a player, after long and intense calculation, becomes mentally exhausted and suddenly makes a blunder or inferior move.
-
B.
Bendii Syndrome
Bendii Syndrome is a rare degenerative neurological illness in the Star Trek universe that affects elderly Vulcans, causing emotional instability and loss of mental control.
-
C.
Vrolik syndrome
Vrolik syndrome, also known as osteogenesis imperfecta type II, is a severe genetic disorder characterized by extremely fragile bones that fracture easily, often leading to perinatal lethality.
-
D.
Florence syndrome
Florence syndrome is a psychosomatic condition in which individuals experience dizziness, rapid heartbeat, confusion, or even hallucinations when exposed to overwhelming art or beauty, particularly in culturally rich cities like Florence.
-
E.
Pompe disease
Pompe disease is a rare inherited metabolic disorder caused by deficiency of the enzyme acid alpha-glucosidase, leading to progressive muscle weakness and cardiomyopathy due to glycogen buildup in cells.
- F. None of above. chosen
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.