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Milroy disease
4 OMIM references -
3 associated genes
12 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal recessive spastic paraplegia type 44
Pelizaeus-Merzbacher-like due to GJC2 mutation
Familial capillary hemangioma
Congenital analbuminemia
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Juvenile myelomonocytic leukemia
LEOPARD syndrome
Metachondromatosis
Noonan syndrome
Synonym(s):
- Hereditary lymphedema type I
- Nonne-Milroy lymphedema
Classification (Orphanet):
- Rare circulatory system disease
- Rare eye disease
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
4 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
FLT4 P35916136352
GJC2 Q5T442608803
VEGFC P49767601528
No signs/symptoms info available.