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MCID: GLS008
MIFTS: 17
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Glossopharyngeal Nerve Disease
Categories:
Neuronal diseases
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Disease Ontology
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A cranial nerve disease that is located in the ninth cranial nerve or its nuclei in the medulla.
MalaCards based summary : Glossopharyngeal Nerve Disease, also known as glossopharyngeal nerve diseases, is related to glossopharyngeal neuralgia and multiple cranial nerve palsy. An important gene associated with Glossopharyngeal Nerve Disease is CRLF1 (Cytokine Receptor Like Factor 1). Affiliated tissues include the ninth cranial nerve or its nuclei in the medulla and cortex, and related phenotypes are Decreased NANOG protein expression and Decreased NANOG protein expression |
Diseases related to Glossopharyngeal Nerve Disease via text searches within MalaCards or GeneCards Suite gene sharing:
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GenomeRNAi Phenotypes related to Glossopharyngeal Nerve Disease according to GeneCards Suite gene sharing:27
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Interventional clinical trials:
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The Foundational Model of Anatomy Ontology organs/tissues related to Glossopharyngeal Nerve Disease:20
The Ninth Cranial Nerve Or Its Nuclei In The Medulla
MalaCards organs/tissues related to Glossopharyngeal Nerve Disease:42
Cortex
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Genes related to Glossopharyngeal Nerve Disease (0 elite genes): - Elite gene
- Cancer Census gene in COSMIC
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Search
GEO
for disease gene expression data for Glossopharyngeal Nerve Disease.
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