Edema
Symptom Information:
Symptom ID: | HPO:0000969 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |