Lymphedema
Symptom Information:
Symptom ID: | HPO:0001004 | ||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||
Quality: | |||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of fluid regulation(HPO:0011032) Edema(HPO:0000969) Lymphedema(HPO:0001004) MedDRA: Vascular disorders(MedDRA:10047065) Lymphatic vessel disorders(MedDRA:10025231) Lymphedema(HPO:0001004) |
||||||||||||||||||||||
Database Frequency: | 62 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA | (OMIM:613623) |
ALG8-CDG | (Orphanet:79325) |
Aarskog-Scott syndrome | (Orphanet:915) |
Alpha-N-acetylgalactosaminidase deficiency | (Orphanet:3137) |
Alpha-N-acetylgalactosaminidase deficiency type 1 | (Orphanet:79279) |
Alpha-N-acetylgalactosaminidase deficiency type 2 | (Orphanet:79280) |
Amniotic bands | (Orphanet:1034) |
Angio-osteohypertrophic syndrome | (Orphanet:2346) |
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema | (Orphanet:69088) |
Aplasia cutis congenita - intestinal lymphangiectasia | (Orphanet:1116) |
Arthrogryposis multiplex congenita | (Orphanet:1037) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Campomelia, Cumming type | (Orphanet:1318) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Castleman disease | (Orphanet:160) |
Cholestasis - lymphedema | (Orphanet:1414) |
Chylous ascites | (Orphanet:1160) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Fabry disease | (Orphanet:324) |
Follicular lymphoma | (Orphanet:545) |
German syndrome | (Orphanet:2077) |
Greenberg dysplasia | (Orphanet:1426) |
HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2 | (OMIM:616006) |
Hennekam syndrome | (Orphanet:2136) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
Idiopathic steroid-sensitive nephrotic syndrome | (Orphanet:69061) |
Juvenile polyposis syndrome | (Orphanet:2929) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA | (OMIM:616342) |
LYMPHEDEMA, HEREDITARY, IB | (OMIM:611944) |
LYMPHEDEMA, HEREDITARY, IC | (OMIM:613480) |
LYMPHEDEMA, HEREDITARY, ID | (OMIM:615907) |
Lethal Kniest-like dysplasia | (Orphanet:2347) |
Lipedema | (Orphanet:77243) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Lymphedema - atrial septal defects - facial changes | (Orphanet:86915) |
Lymphedema - cerebral arteriovenous anomaly | (Orphanet:86914) |
Lymphedema - distichiasis | (Orphanet:33001) |
MPI-CDG | (Orphanet:79319) |
Melorheostosis | (Orphanet:2485) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Monosomy 18p | (Orphanet:1598) |
Monosomy 22q13 | (Orphanet:48652) |
Mucopolysaccharidosis type 7 | (Orphanet:584) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Multiple epiphyseal dysplasia, Al-Gazali type | (Orphanet:166024) |
NOONAN SYNDROME 1 | (OMIM:163950) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
POEMS syndrome | (Orphanet:2905) |
Proteus syndrome | (Orphanet:744) |
Proximal spinal muscular atrophy | (Orphanet:70) |
Pterygium colli - intellectual deficit - digital anomalies | (Orphanet:2988) |
Schneckenbecken dysplasia | (Orphanet:3144) |
Secondary intestinal lymphangiectasia | (Orphanet:90363) |
Toriello-Lacassie-Droste syndrome | (Orphanet:3339) |
Turner syndrome | (Orphanet:881) |
Wilson-Turner syndrome | (Orphanet:3459) |
Yellow nail syndrome | (Orphanet:662) |