Lymphedema

Symptom Information:

Symptom ID: HPO:0001004
Synonyms:
Lymphoedema [HPO:0001004]
Onset of lymphedema around puberty [HPO:0001004]
Lymphedema (disorder) [Orphanet:36750]
Lymphatic edema (morphologic abnormality) [Orphanet:36750]
LYMPHOEDEMA [HPO:0001004]
Lymphedema [Orphanet:36750]
Lymphedema [OMIM:Lymphedema]
Onset of lymphedema around puberty [OMIM:Onset of lymphedema around puberty]
Lymphoedema [Orphanet:36750]
Lymphoedema [MedDRA:10025282]
Lymphedema [MedDRA:10025282]
Lymphoedema NOS [MedDRA:10025282]
Lymphoedema praecox [MedDRA:10025282]
Other lymphedema [MedDRA:10025282]
Other lymphoedema [MedDRA:10025282]
Localised accumulation of lymphatic fluid [MedDRA:10025282]
Lymphedema praecox [MedDRA:10025282]
Localized accumulation of lymphatic fluid [MedDRA:10025282]
Lymphedema (lower extremities) [OMIM:Lymphedema (lower extremities)]
Lymphedema (lower limb) [OMIM:Lymphedema (lower limb)]
Lymphedema (lower limbs) [OMIM:Lymphedema (lower limbs)]
Lymphoedemas [MedDRA:10052790]
Quality:
Cross references:
Orphanet:36750 "Lymphedema" [Orphanet:36750]
OMIM: "Lymphedema" [OMIM:Lymphedema]
OMIM: "Onset of lymphedema around puberty" [OMIM:Onset of lymphedema around puberty]
OMIM: "Lymphedema (lower extremities)" [OMIM:Lymphedema (lower extremities)]
OMIM: "Lymphedema (lower limb)" [OMIM:Lymphedema (lower limb)]
OMIM: "Lymphedema (lower limbs)" [OMIM:Lymphedema (lower limbs)]
UMLS:C0024236 "LYMPHOEDEMA" [HPO:0001004]
UMLS:C0024236 "Lymphedema" [Orphanet:36750]
Is a (Direct Parents):
MedDRA Lymphatic vessel disorders
Orphanet Abnormality of the lymphatic system
HPO         Edema
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)