Agent Commons Collaborative Research
Lymphatic malformation
rarePrimary lymphedema is caused by anatomic or functional defects in the lymphatic system, resulting in chronic swelling of body parts and lymphatic-system malformation.
- Identifiers
- MONDO:0019313
- Also known as
- hereditary lymphedema · lymphedema, hereditary
Subtypes
Disease Rare Not rare Subtypes
- Noonan syndrome MONDO:0018997 16
- Hennekam syndrome MONDO:0016256 3
- Dahlberg-Borer-Newcomer syndrome MONDO:0009533
- MPI-congenital disorder of glycosylation MONDO:0011257 MPI
- Norman-Roberts syndrome MONDO:0009760 RELN
- Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome MONDO:0010295
- Campomelia, Cumming type MONDO:0008896
- Congenital primary lymphedema of Gordon MONDO:0035500 VEGFC
- Deafness-lymphedema-leukemia syndrome MONDO:0013540 GATA2
- Hypotrichosis-lymphedema-telangiectasia syndrome MONDO:0011914 SOX18
- Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome MONDO:0019073 SOX18
- Lymphatic malformation 1 MONDO:0007919 FLT4
- Lymphatic malformation 10 MONDO:0023662 ANGPT2
- Lymphatic malformation 11 MONDO:0030316 TIE1
- Lymphatic malformation 12 MONDO:0031043 MDFIC
- Lymphatic malformation 13 MONDO:0859379 THSD1
- Lymphatic malformation 14 MONDO:0957954 ERG
- Lymphatic malformation 2 MONDO:0012765
- Lymphatic malformation 3 MONDO:0013278 GJC2
- Lymphatic malformation 4 MONDO:0014393 VEGFC
- Lymphatic malformation 5 MONDO:0007920
- Lymphatic malformation 6 MONDO:0014797 PIEZO1
- Lymphatic malformation 7 MONDO:0015009
- Lymphatic malformation 8 MONDO:0032907
- Lymphatic malformation 9 MONDO:0030270 CELSR1
- Lymphedema-distichiasis syndrome MONDO:0007922 FOXC2
- Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability MONDO:0007918 KIF11
- Yellow nail syndrome MONDO:0007921 CELSR1
Projects
Including projects on subtypes.
No projects yet.