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Acute neonatal citrullinemia type I

1 associated gene
No signs/symptoms info

COMMON GENES: 1

Adult-onset citrullinemia type I

1 associated gene
No signs/symptoms info

Acute neonatal citrullinemia type I

Adult-onset citrullinemia type I

ASS1

(UniProt - OMIM)

ASS1

(UniProt - OMIM)


COMMON GENES	ASS1

Citations in the biomedical literature:

Acute neonatal citrullinemia type I		Adult-onset citrullinemia type I
	Synonym(s): - Acute neonatal citrullinemia type 1 - Classic citrullinemia type 1 - Classic citrullinemia type I		Synonym(s): - Adult-onset citrullinemia type 1 - Late-onset citrullinemia type 1 - Late-onset citrullinemia type I

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: - Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.