Open spinal dysraphism

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Open spinal dysraphism

ORPHA:268369Clinical group

Also called Open spina bifida · Spina bifida aperta

What it is

A rare neural tube closure defect characterized by a skin defect with exposed neural tissue in the area of the spinal column, with or without a protruding sac at the location of the defect. Signs and symptoms are variable depending on the content (only meninges or also spinal cord tissue), location, and severity of the lesion, but may include motor, sensory, and/or sphincter dysfunction, hydrocephalus, and/or skeletal anomalies (e. g. scoliosis, hemivertebrae), among others.

Key facts

Prevalence
1-5 / 10 000 (at birth, Germany)
Age of onset
Infancy, Neonatal
Inheritance
Multigenic/multifactorial, Not applicable
Classified as
Clinical group

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

ICD-10 codes

Q05.0filed under a broader ICD-10 category — shared with 1 other rare disease
Q05.1filed under a broader ICD-10 category — shared with 1 other rare disease
Q05.2filed under a broader ICD-10 category — shared with 2 other rare diseases
Q05.3filed under a broader ICD-10 category — shared with 2 other rare diseases
Q05.4filed under a broader ICD-10 category — shared with 1 other rare disease
Q05.5filed under a broader ICD-10 category — shared with 1 other rare disease
Q05.6filed under a broader ICD-10 category — shared with 1 other rare disease
Q05.7filed under a broader ICD-10 category — shared with 2 other rare diseases
Q05.8filed under a broader ICD-10 category — shared with 2 other rare diseases
Q05.9filed under a broader ICD-10 category — shared with 5 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Benefit programs to look at

Programs whose eligibility touches the same ICD-10 categories. Eligibility is decided by the administering agency, never by this page.

Cross-references

MONDO 0017062MONDO 17062UMLS C0917813

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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