ORPHA:645354

Saccular limited dorsal myeloschisis

Synonyms: Saccular LDM

Type: Morphological anomaly
Group: Disorder
Inheritance: Unknown
Status: active

A rare form of limited dorsal myeloschisis (LDM), characterized by the stalk attached to the apex of a fully epithelialized meningocele. Chiari II malformation is not present.

Names in Orphadata languages

10 of 12 languages

Lang	Name	Synonyms
en	Saccular limited dorsal myeloschisis	Saccular LDM
fr	Myéloschisis dorsal limité sacculaire	LDM sacculaire
de	Sakkuläre begrenzte dorsale Myeloschisis	Sakkuläre LDM
es	Mielosquisis dorsal limitada sacular	MDL sacular
it	Mieloschisi sacculare limitata al dorso	LDM sacculare
nl	Sacculaire beperkte dorsale myeloschisis	Sacculaire LDM
pt	Mielosquisis sacular dorsal limitada	LDM sacular
pl	Workowaty ograniczony rozszczep części grzbietowej rdzenia kręgowego	= en
cs	Sakulární omezená dorzální myeloschíza	= en
uk	Саккулярний обмежений дорсальний мієлошизис	Сакральний LDM

Definition in:

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	Q76.0	NTBT	attributed	validated
MONDO	0970963	E		validated
MONDO	970963	E		validated
UMLS	C5816715	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (1):

ORPHA:645319Saccular spinal dysraphism with a stalk to the dome
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases

No children.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/645354
This record as JSON: /data/d/645354.json