ODCs

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

PROTEIN INTERACTIONS: 1

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

Terminal osseous dysplasia - pigmentary defects

Acute necrotizing encephalopathy of childhood

FLNA	(UniProt - OMIM)		CPT2	(UniProt - OMIM)
			RANBP2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA	(0.49)	RANBP2

Citations in the biomedical literature:

Terminal osseous dysplasia - pigmentary defects		Acute necrotizing encephalopathy of childhood
	Synonym(s): (no synonyms)		Synonym(s): - ANEC - Isolated ANE - Isolated acute necrotizing encephalopathy

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: x-linked dominant		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: sporadic

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

No signs/symptoms info available.