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Congenital analbuminemia
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial drusen
2 OMIM references -
2 associated genes
No signs/symptoms info
Congenital analbuminemia
Familial drusen

ALB
(UniProt - OMIM)
 CFH
(UniProt - OMIM)
EFEMP1
(UniProt - OMIM)

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


Citations in the biomedical literature:


Congenital analbuminemia
ALB
Familial drusen
CFH EFEMP1



Congenital analbuminemia
Familial drusen

Synonym(s):
(no synonyms)

Synonym(s):
- DHRD
- Dominant drusen
- Dominant radial drusen
- Doyne honeycomb retinal dystrophy
- Malattia leventinese
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -
Classification (ICD10):
- Diseases of the eye and adnexa -
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: normal
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.