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Total spina bifida cystica

6 associated genes
No signs/symptoms info

COMMON GENES: 1

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

Total spina bifida cystica

Chordoma

FUZ	(UniProt - OMIM)		T	(UniProt - OMIM)
MTHFD1	(UniProt - OMIM)
MTHFR	(UniProt - OMIM)
T	(UniProt - OMIM)
VANGL1	(UniProt - OMIM)
VANGL2	(UniProt - OMIM)


COMMON GENES	T

Citations in the biomedical literature:

Total spina bifida cystica		Chordoma
	Synonym(s): (no synonyms)		Synonym(s): - Notochordal sarcoma

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

	Classification (ICD10): (no data available)		Classification (ICD10): (no data available)

	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: <1 / 1 000 000 Average age onset: adulthood Average age of death: any age Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D002817

No signs/symptoms info available.