Edema

Symptom Information:

Symptom ID: HPO:0000969
Synonyms:
Hydrops [HPO:0000969]
Oedema [HPO:0000969]
Edema [OMIM:Edema]
Hydrops [OMIM:Hydrops]
Edema (hands and feet) [OMIM:Edema (hands and feet)]
Oedema [MedDRA:10030095]
Quality:
Cross references:
OMIM: "Edema" [OMIM:Edema]
OMIM: "Hydrops" [OMIM:Hydrops]
OMIM: "Edema (hands and feet)" [OMIM:Edema (hands and feet)]
UMLS:C0013604 "Edema" [HPO:0000969]
Is a (Direct Parents):
HPO         Macular edema
HPO         Abnormality of fluid regulation
MedDRA Total fluid volume increased
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)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Electrolyte and fluid balance conditions(MedDRA:10014412)
       Total fluid volume increased(MedDRA:10044085)
          Edema(HPO:0000969)
Database Frequency: 117 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis type 1A (Orphanet:93299)
Achondrogenesis type 1B (Orphanet:93298)
Achondrogenesis type 2 (Orphanet:93296)
Acquired angioedema (Orphanet:91385)
Antisynthetase syndrome (Orphanet:81)
Autosomal dominant beta2-microglobulinic amyloidosis (Orphanet:314652)
Autosomal recessive limb-girdle muscular dystrophy type 2E (Orphanet:119)
BARTTER SYNDROME, TYPE 4B (OMIM:613090)
CARDIAC VALVULAR DEFECT, DEVELOPMENTAL (OMIM:212093)
CINCA syndrome (Orphanet:1451)
CLUSTER HEADACHE, FAMILIAL (OMIM:119915)
COENZYME Q10 DEFICIENCY, PRIMARY, 3 (OMIM:614652)
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2 (OMIM:610158)
CREST syndrome (Orphanet:90290)
Cardiomyopathy, dilated, 1Y (OMIM:611878)
Castleman disease (Orphanet:160)
Cerebroretinal vasculopathy (Orphanet:3421)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Classical mycosis fungoides (Orphanet:2584)
Combined oxidative phosphorylation defect type 2 (Orphanet:254920)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Congenital nephrotic syndrome, Finnish type (Orphanet:839)
Cushing disease (Orphanet:96253)
Cutaneous lupus erythematosus (Orphanet:535)
DEAFNESS, UNILATERAL, WITH DELAYED ENDOLYMPHATIC HYDROPS (OMIM:612097)
Dermatitis herpetiformis (Orphanet:1656)
Dermatomyositis (Orphanet:221)
Dissecting cellulitis of the scalp (Orphanet:345)
EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL (OMIM:129840)
ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY (OMIM:600351)
ENTEROPATHY, PROTEIN-LOSING (OMIM:226300)
Eosinophilic fasciitis (Orphanet:3165)
Erythropoietic protoporphyria (Orphanet:79278)
FIBROCHONDROGENESIS 1 (OMIM:228520)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1 (OMIM:603278)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 (OMIM:614131)
Fabry disease (Orphanet:324)
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation (Orphanet:93214)
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes (Orphanet:93216)
Familial isolated dilated cardiomyopathy (Orphanet:154)
Familial multiple nevi flammei (Orphanet:624)
Fountain syndrome (Orphanet:3219)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form (Orphanet:308621)
HERNS syndrome (Orphanet:63261)
Hawkinsinuria (Orphanet:2118)
Hereditary angioedema (Orphanet:91378)
Hereditary vascular retinopathy (Orphanet:71291)
Hypotonia with lactic acidemia and hyperammonemia (Orphanet:137908)
Hypouricemia, renal, 1 (OMIM:220150)
Idiopathic copper-associated cirrhosis (Orphanet:209919)
Immunoglobulin A vasculitis (Orphanet:761)
Infant acute respiratory distress syndrome (Orphanet:70587)
Infantile Bartter syndrome with deafness (Orphanet:89938)
Insulin-resistance syndrome type A (Orphanet:2297)
Johanson-Blizzard syndrome (Orphanet:2315)
Kaposi's sarcoma (Orphanet:33276)
Kawasaki disease (Orphanet:2331)
Klippel-Trénaunay syndrome (Orphanet:90308)
Leigh syndrome with nephrotic syndrome (Orphanet:255249)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lethal congenital contracture syndrome type 1 (Orphanet:1486)
Lethal congenital contracture syndrome type 2 (Orphanet:137776)
Lethal multiple pterygium syndrome (Orphanet:33108)
MERRF (Orphanet:551)
MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUALAPPEARANCE (OMIM:612947)
Majeed syndrome (Orphanet:77297)
McKusick-Kaufman syndrome (Orphanet:2473)
Melkersson-Rosenthal syndrome (Orphanet:2483)
Mevalonic aciduria (Orphanet:29)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Multiple benign circumferential skin creases on limbs (Orphanet:2505)
NEPHROTIC SYNDROME, TYPE 2 (OMIM:600995)
NEPHROTIC SYNDROME, TYPE 3 (OMIM:610725)
NEPHROTIC SYNDROME, TYPE 8 (OMIM:615244)
NEPHROTIC SYNDROME, TYPE 9 (OMIM:615573)
Neonatal hemochromatosis (Orphanet:446)
Nephronophthisis 1 (OMIM:256100)
Nodular non-suppurative panniculitis (Orphanet:33577)
Non-histaminic angioedema (Orphanet:658)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Omenn syndrome (Orphanet:39041)
Opsismodysplasia (Orphanet:2746)
PEHO syndrome (Orphanet:2836)
PREECLAMPSIA/ECLAMPSIA 1 (OMIM:189800)
PROTOPORPHYRIA, ERYTHROPOIETIC (OMIM:177000)
Pachydermoperiostosis (Orphanet:2796)
Pediatric systemic sclerosis (Orphanet:93567)
Perlman syndrome (Orphanet:2849)
Pierson syndrome (Orphanet:2670)
Pontocerebellar hypoplasia type 6 (Orphanet:166073)
Porphyria cutanea tarda (Orphanet:101330)
Preeclampsia (Orphanet:275555)
Renal coloboma syndrome (Orphanet:1475)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
Sarcoidosis (Orphanet:797)
Sea-blue histiocytosis (Orphanet:158029)
Senile systemic amyloidosis (Orphanet:330001)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Superficial epidermolytic ichthyosis (Orphanet:455)
Systemic sclerosis (Orphanet:90291)
Sézary syndrome (Orphanet:3162)
TRAPS syndrome (Orphanet:32960)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Thoracic outlet syndrome (Orphanet:97330)
Thymic carcinoma (Orphanet:99868)
Thymic epithelial neoplasm (Orphanet:3398)
Thymic tumor (Orphanet:100100)
Transaldolase deficiency (Orphanet:101028)
Wells syndrome (Orphanet:901)
Wilson disease (Orphanet:905)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
X-linked lethal multiple pterygium syndrome (Orphanet:79447)