ODCs

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6 associated genes
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Thoracolumbosacral spina bifida cystica

Arnold-Chiari malformation type II

Citations in the biomedical literature:

Thoracolumbosacral spina bifida cystica		Arnold-Chiari malformation type II
	Synonym(s): (no synonyms)		Synonym(s): - Arnold-Chiari malformation type 2 - Chiari malformation type 2 - Chiari malformation type II

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: multigenic/multifactorial		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: no data available Type of inheritance: sporadic

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.