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Autosomal recessive spastic paraplegia type 44
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Milroy disease
4 OMIM references -
3 associated genes
No signs/symptoms info
Autosomal recessive spastic paraplegia type 44
Milroy disease

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

COMMON
GENES 		GJC2


Citations in the biomedical literature:


Autosomal recessive spastic paraplegia type 44
GJC2
Milroy disease
FLT4 VEGFC



Autosomal recessive spastic paraplegia type 44
Milroy disease

Synonym(s):
- SPG44
Synonym(s):
- Hereditary lymphedema type I
- Nonne-Milroy lymphedema
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare eye disease
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
4 OMIM references -
No MeSH references
No signs/symptoms info available.