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Congenital analbuminemia
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Adenosine monophosphate deaminase deficiency
2 OMIM references -
2 associated genes
1 sign/symptom
Congenital analbuminemia
Adenosine monophosphate deaminase deficiency

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

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


Citations in the biomedical literature:


Congenital analbuminemia
ALB
Adenosine monophosphate deaminase deficiency
AMPD1 AMPD3



Congenital analbuminemia
Adenosine monophosphate deaminase deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- AMP deaminase deficiency
- Myoadenylate deaminase deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C538234
Adenosine monophosphate deaminase deficiency

Very frequent
- Autosomal recessive inheritance



Congenital analbuminemia

(no data available)