ORPHA:645343
Non-saccular limited dorsal myeloschisis
Synonyms: Flat LDM · Non-saccular LDM
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Unknown
- Status
- active
A rare form of limited dorsal myeloschisis (LDM), characterized by a non saccular cutaneous stigmata (midline skin abnormality classically dimple, pit or sometimes angioma), the stalk is attached to this cutaneous stigmata. Fibroneural stalk varies in thickness and complexity.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-saccular limited dorsal myeloschisis | Flat LDM · Non-saccular LDM |
| fr | Myéloschisis dorsal limité non-sacculaire | LDM non sacculaire · LDM plat |
| de | Nicht-sakkuläre begrenzte dorsale Myeloschisis | Flache LDM · Nicht-sakkuläre LDM |
| es | Mielosquisis dorsal limitada no sacular | MDL no sacular · MDL plana |
| it | Mieloschisi non sacculare limitata al dorso | LDM non sacculare · LDM piatta |
| nl | Niet-sacculaire beperkte dorsale myeloschisis | Niet-sacculaire LDM · Platte LDM |
| pt | Mielosquisis não-sacular dorsal limitada | LDM não-sacular · LDM plana |
| pl | Nieworkowaty ograniczony rozszczep grzbietowej części rdzenia kręgowego | = en |
| cs | Omezená dorzální myeloschíza bez vaku | = en |
| uk | Несакральний обмежений дорсальний мієлошизис | Плоский LDM · Несакральна LDM |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q76.0 | NTBT | attributed | validated |
| MONDO | 0968989 | E | validated | |
| MONDO | 968989 | E | validated | |
| UMLS | C5816717 | 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:645196Limited dorsal myeloschisis
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
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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/645343
- This record as JSON: /data/d/645343.json