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Congenital analbuminemia
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
1 associated gene
No signs/symptoms info
Congenital analbuminemia
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

ALB
(UniProt - OMIM)
 DMD
(UniProt - OMIM)

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


Citations in the biomedical literature:


Congenital analbuminemia
ALB
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
DMD



Congenital analbuminemia
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare cardiac disease
- 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: adulthood
Average age of death: -
Type of inheritance: x-linked dominant
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.