Preferred Name |
Fragile X Syndrome |
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Synonyms |
Organ_System: nervous system PathwayType: signaling Notes: FMR1 gene mutations are associated with the development of autism symptoms in patients with Fragile X Syndrome. Link: https://mammal-profservices.pathwaystudio.com/app/sd?urn=urn:agi-pathway:uuid-9be5bc9f-9562-43d4-b4dd-2c7139c1c587 PMID: 27690107 PMID: 27672537 NodeType: Pathway Pathway_Author: E. Klimov ORCID:0000-0003-2674-5783 Description: The role of mutations in the FMR1 gene in the development of autism symptoms of Fragile X Syndrome. Pathway is built manually using published studies. Source: Diseases |
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ID |
urn:agi-pathway:uuid-9be5bc9f-9562-43d4-b4dd-2c7139c1c587 |
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database_cross_reference |
PS:PathwayType PS:Description PS:Pathway_Author PS:Link PS:Organ_System PS:PMID PS:NodeType PS:Notes PS:Source |
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has_exact_synonym |
Organ_System: nervous system PathwayType: signaling Notes: FMR1 gene mutations are associated with the development of autism symptoms in patients with Fragile X Syndrome. PMID: 27690107 PMID: 27672537 NodeType: Pathway Pathway_Author: E. Klimov ORCID:0000-0003-2674-5783 Description: The role of mutations in the FMR1 gene in the development of autism symptoms of Fragile X Syndrome. Pathway is built manually using published studies. Source: Diseases |
|
id |
urn:agi-pathway:uuid-9be5bc9f-9562-43d4-b4dd-2c7139c1c587 |
|
label |
Fragile X Syndrome |
|
notation |
uuid-9be5bc9f-9562-43d4-b4dd-2c7139c1c587 |
|
prefLabel |
Fragile X Syndrome |
|
treeView |
urn:agi-folder:fragile_x_syndrome urn:agi-folder:nervous_system urn:agi-folder:f |
|
subClassOf |
urn:agi-folder:fragile_x_syndrome urn:agi-folder:nervous_system urn:agi-folder:f |