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

Ketoacidosis due to beta-ketothiolase deficiency

Isolated growth hormone deficiency type IB

ACAT1	(UniProt - OMIM)		GH1	(UniProt - OMIM)
			GHRHR	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACAT1	(0.63)	GH1

Citations in the biomedical literature:

Ketoacidosis due to beta-ketothiolase deficiency		Isolated growth hormone deficiency type IB
	Synonym(s): - Alpha-methyl-acetoacetyl-CoA thiolase deficiency		Synonym(s): - Congenital IGHD type IB - Congenital isolated GH deficiency type IB - Congenital isolated growth hormone deficiency type IB

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		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 recessive		Epidemiological data: Class of prevalence: - Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.