ORPHA:221117
Gerstmann syndrome
- Type
- Disease
- Group
- Disorder
- Status
- active
Gerstmann syndrome is a very rare neurological disorder characterized by the specific association of acalculia, finger agnosia, left-right disorientation, and agraphia, which is supposed to be secondary to a focal subcortical white matter damage in the parietal lobe.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Gerstmann syndrome | |
| fr | Syndrome de Gerstmann | |
| de | Gerstmann-Syndrom | |
| es | Síndrome de Gerstmann | |
| it | Sindrome di Gerstmann | |
| nl | Syndroom van Gerstmann | |
| pt | Síndrome de Gerstmann | |
| pl | Zespół Gerstmanna | |
| cs | Gerstmannův syndrom | |
| uk | Синдром Герстмана | |
| zh | 格斯特曼综合征 | |
| tr | Gerstmann sendromu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | F81.2 | NTBT | inclusion | validated |
| ICD-11 | MB4C | E | specific | validated |
| MONDO | 0005773 | E | validated | |
| MeSH | D005862 | E | validated | |
| UMLS | C0017494 | E | validated | |
| GARD | 8660 | E | validated | |
| MedDRA | 10048608 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98006Rare neurologic disease
rare neurological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/221117
- This record as JSON: /data/d/221117.json