ORPHA:715025

Spinal fast-flow vascular malformation

Synonyms: Spinal arteriovenous malformation · Spinal arteriovenous shunt

Type: Clinical group
Group: Group of disorders
Status: active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Names in Orphadata languages

9 of 12 languages

Lang	Name	Synonyms
en	Spinal fast-flow vascular malformation	Spinal arteriovenous malformation · Spinal arteriovenous shunt
fr	Malformation vasculaire spinale à flux rapide	Malformation artérioveineuse spinale
de	Spinale schnell-fließende vaskuläre Fehlbildung	Spinale arteriovenöse Gefäßmalformation · Spinale arteriovenöse fast-flow Malformation · Spinale Gefäßmalformation mit arteriovenösem Shunt
es	Malformación vascular espinal de alto flujo	Malformación arteriovenosa espinal · Derivación arteriovenosa espinal
it	Malformazione vascolare spinale a flusso rapido	Malformazione arterovenosa spinale · Shunt arterovenoso spinale
nl	Spinale fast-flow vasculaire malformatie	Spinale arterioveneuze malformatie · Spinale arterioveneuze fistel · Spinale arterioveneuze shunt · Vaatmalformatie van ruggenmerg met snelle bloedstroom
pt	Spinal fast-flow malformation
pl	Malformacja rdzenia kręgowego z szybkim przepływem	= en
cs	Spinal fast-flow vascular malformation	= en

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:98006Rare neurologic disease

Parents in the classifications (2):

ORPHA:715744Fast-flow vascular malformation of the central nervous system
rare developmental anomalies during embryogenesis; rare circulatory system diseases
ORPHA:102006Neurovascular malformation
rare neurological diseases

Children (6):

Codes that Orphanet moved or referred to this one:

ORPHA:79093OBSOLETE: Foix-Alajouanine syndrome referred to · inactive

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

33 annotations · validated 2025-10-14

HPO	Term (as annotated by Orphanet)	Diagnostic
Very frequent (99-80%)
HP:0012703	Abnormal subarachnoid space morphology
HP:0000707	Abnormality of the nervous system
HP:0004947	Arteriovenous fistula
HP:0040272	Hyperintensity of MRI T2 signal of the spinal cord
HP:0002196	Myelopathy
HP:0100561	Spinal cord lesion
HP:0012721	Venous malformation
Frequent (79-30%)
HP:0001284	Areflexia
HP:0003418	Back pain
HP:0001347	Hyperreflexia
HP:0001324	Muscle weakness
HP:0012486	Myelitis
HP:0007199	Progressive spastic paraparesis
Occasional (29-5%)
HP:0002607	Bowel incontinence
HP:0012423	Colonic inertia
HP:0009053	Distal lower limb muscle weakness
HP:0012534	Dysesthesia
HP:0030014	Female sexual dysfunction
HP:0002359	Frequent falls
HP:0000009	Functional abnormality of the bladder
HP:0001288	Gait disturbance
HP:0002141	Gait imbalance
HP:0003419	Low back pain
HP:0007340	Lower limb muscle weakness
HP:0040307	Male sexual dysfunction
HP:0000011	Neurogenic bladder
HP:0003401	Paresthesia
HP:0003474	Somatic sensory dysfunction
HP:0002317	Unsteady gait
HP:0000020	Urinary incontinence
HP:0000016	Urinary retention
Very rare (<4-1%)
HP:0002318	Cervical myelopathy
HP:0008944	Distal lower limb amyotrophy

Run the differential on the 7 obligate / very frequent terms

Annotation source: 34178190[PMID]_28673891[PMID]_33457368[PMID]

Sources for this card

Orphanet page: orpha.net/en/disease/detail/715025
This record as JSON: /data/d/715025.json