ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Developmental and speech delay due to SOX5 deficiency

FTH1-related iron overload


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SOX5	(0.63)	FTH1

Citations in the biomedical literature:

Developmental and speech delay due to SOX5 deficiency		FTH1-related iron overload
	Synonym(s): (no synonyms)		Synonym(s): - FTH1-associated iron overload

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hepatic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

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

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

No signs/symptoms info available.