eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| gerstmann syndrome | ||||
| Disease ID | 1552 |
|---|---|
| Disease | gerstmann syndrome |
| Definition | A disorder of cognition characterized by the tetrad of finger agnosia, dysgraphia, DYSCALCULIA, and right-left disorientation. The syndrome may be developmental or acquired. Acquired Gerstmann syndrome is associated with lesions in the dominant (usually left) PARIETAL LOBE which involve the angular gyrus or subjacent white matter. (From Adams et al., Principles of Neurology, 6th ed, p457) |
| Synonym | angular gyrus syndrome aphasia-angular gyrus syndrome aphasia-angular gyrus syndrome (disorder) de gerstmann, syndrome finger-agnosia-left-right-confusion-acalculia-agraphia finger-agnosia-left-right-confusion-acalculia-agraphias gerstmann badal syndrome gerstmann syndrome [disease/finding] gerstmann's syndrome gerstmann, syndrome de gerstmann-badal syndrome gerstmanns syndrome syndrome de gerstmann syndrome, gerstmann syndrome, gerstmann-badal |
| Orphanet | |
| DOID | |
| UMLS | C0017494 |
| MeSH | |
| SNOMED-CT | |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:1) |
| Locus | (Waiting for update.) |
| Disease ID | 1552 |
|---|---|
| Disease | gerstmann syndrome |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:6) HP:0010523 | Alexia | 1 HP:0030784 | Anomic aphasia | 1 HP:0030049 | Brain abscess | 1 HP:0001289 | Confusion | 1 HP:0002442 | Dyscalculia | 1 HP:0010524 | Agnosia | 1 |
| Disease ID | 1552 |
|---|---|
| Disease | gerstmann syndrome |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:1) C1262195 | echoacousia |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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Text Mining Genotype(Total Genotypes:0) | |
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All Snps(Total Genotypes:0) | |
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GWASdb Annotation(Total Genotypes:0) | |
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| (Waiting for update.) | |
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.) |
| Disease ID | 1552 |
|---|---|
| Disease | gerstmann syndrome |
| Case | (Waiting for update.) |