charles bonnet syndrome |
Disease ID | 1943 |
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Disease | charles bonnet syndrome |
Synonym | charles bonnet syndrome (disorder) |
UMLS | C0339731 |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:8) C0014544 | epilepsy | 2 C0024437 | macular degeneration | 2 C0036454 | visual field defect | 1 C0036454 | visual field defects | 1 C0011884 | diabetic retinopathy | 1 C0015397 | ocular disease | 1 C0024437 | age-related macular degeneration | 1 C0035305 | retinal detachment | 1 |
Curated Gene | (Waiting for update.) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | (Waiting for update.) |
Locus | (Waiting for update.) |
Disease ID | 1943 |
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Disease | charles bonnet syndrome |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:9) HP:0002367 | Visual hallucinations | 5 HP:0000738 | Sensory hallucination | 4 HP:0000608 | Macular degeneration | 2 HP:0000708 | Behavioral problems | 1 HP:0002664 | Neoplasia | 1 HP:0000505 | Poor vision | 1 HP:0000541 | Detached retina | 1 HP:0007868 | ARMD | 1 HP:0001123 | Partial loss of field of vision | 1 |
Disease ID | 1943 |
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Disease | charles bonnet syndrome |
Manually Symptom | UMLS | Name(Total Manually Symptoms:3) |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:2) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
All Snps(Total Genotypes:0) | |
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GWASdb Annotation(Total Genotypes:0) | |
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GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Chemical(Total Drugs:0) | |
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FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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(Waiting for update.) |