ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Fibrosarcoma

Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression

ETV6	(UniProt - OMIM)		TNK2	(UniProt - OMIM)
NTRK3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NTRK3	(0.63)	TNK2

Citations in the biomedical literature:

Fibrosarcoma		Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression

	Classification (Orphanet): - Rare bone disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - 1 MeSH reference: D005354		External references: No OMIM references No MeSH references

No signs/symptoms info available.