ODCs

Cytoscape Web

Click node...

Adenosine monophosphate deaminase deficiency

2 OMIM references -
2 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

Congenital analbuminemia

1 associated gene
No signs/symptoms info

Adenosine monophosphate deaminase deficiency

Congenital analbuminemia

AMPD1	(UniProt - OMIM)		ALB	(UniProt - OMIM)
AMPD3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	AMPD3	(0.72)	ALB

Citations in the biomedical literature:

Adenosine monophosphate deaminase deficiency		Congenital analbuminemia
	Synonym(s): - AMP deaminase deficiency - Myoadenylate deaminase deficiency		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

	External references: 2 OMIM references - 1 MeSH reference: C538234		External references: No OMIM references No MeSH references

Adenosine monophosphate deaminase deficiency
	Very frequent - Autosomal recessive inheritance
Congenital analbuminemia
(no data available)