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Milroy disease
4 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital analbuminemia
1 associated gene
No signs/symptoms info
Milroy disease
Congenital analbuminemia

FLT4
(UniProt - OMIM)
 ALB
(UniProt - OMIM)
GJC2
(UniProt - OMIM)
VEGFC
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GJC2
(0.72)
ALB


Citations in the biomedical literature:


Milroy disease
FLT4 GJC2 VEGFC
Congenital analbuminemia
ALB



Milroy disease
Congenital analbuminemia

Synonym(s):
- Hereditary lymphedema type I
- Nonne-Milroy lymphedema
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare circulatory system disease
- Rare eye disease
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
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:
4 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.