All diseases

OMIM ID
153100
OMIM term:
LYMPHEDEMA, HEREDITARY, IA
Alternative terms:
LMPH1A
NONNE-MILROY LYMPHEDEMA
MILROY DISEASE
LYMPHEDEMA, EARLY-ONSET
PRIMARY CONGENITAL LYMPHEDEMA; PCL
(∗) Location:
5q35.3  
(†) Associated OMIM genes:
FLT4  
(‡) Associated MGI genes:
Flt4  

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