ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Myelofibrosis with myeloid metaplasia

Acute neonatal citrullinemia type I


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	JAK2	(0.63)	ASS1

Citations in the biomedical literature:

Myelofibrosis with myeloid metaplasia		Acute neonatal citrullinemia type I
	Synonym(s): - Agnogenic myeloid metaplasia - Idiopathic myelofibrosis - Myelosclerosis with myeloid metaplasia - Primary myelofibrosis		Synonym(s): - Acute neonatal citrullinemia type 1 - Classic citrullinemia type 1 - Classic citrullinemia type I

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

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

	Epidemiological data: (no data available)		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: No OMIM references No MeSH references

No signs/symptoms info available.