PSNP3
MCID: SPR048
MIFTS: 11
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Supranuclear Palsy, Progressive, 3 (PSNP3)
Categories:
Eye diseases, Genetic diseases, Neuronal diseases, Rare diseases
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MalaCards integrated aliases for Supranuclear Palsy, Progressive, 3:
Classifications:
MalaCards categories:
Global: Genetic diseases Rare diseases Anatomical: Eye diseases Neuronal diseases |
MalaCards based summary
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Supranuclear Palsy, Progressive, 3, also known as psnp3, is related to perrault syndrome 1 and supranuclear palsy, progressive, 1. An important gene associated with Supranuclear Palsy, Progressive, 3 is PSNP3 (Supranuclear Palsy, Progressive, 3). Affiliated tissues include eye.
Description from OMIM:
610898
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Diseases in the Supranuclear Palsy, Progressive, 1 family:
Diseases related to Supranuclear Palsy, Progressive, 3 via text searches within MalaCards or GeneCards Suite gene sharing:
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MalaCards organs/tissues related to Supranuclear Palsy, Progressive, 3:41
Eye
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Search
GEO
for disease gene expression data for Supranuclear Palsy, Progressive, 3.
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