Edema of the lower limbs
Symptom Information:
Symptom ID: | HPO:0010741 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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) Edema of the lower limbs(HPO:0010741) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Electrolyte and fluid balance conditions(MedDRA:10014412) Total fluid volume increased(MedDRA:10044085) Edema of the lower limbs(HPO:0010741) |
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Database Frequency: | 34 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ATTRV122I amyloidosis | (Orphanet:85451) |
Alport syndrome | (Orphanet:63) |
Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERALVASCULATURE | (OMIM:126320) |
Fabry disease | (Orphanet:324) |
Familial Mediterranean fever | (Orphanet:342) |
Fibronectin glomerulopathy | (Orphanet:84090) |
Galactosemia | (Orphanet:352) |
Gaucher disease type 1 | (Orphanet:77259) |
Griscelli disease | (Orphanet:381) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hughes-Stovin syndrome | (Orphanet:228116) |
Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
Intestinal lymphangiectasia | (Orphanet:36204) |
Kaposi's sarcoma | (Orphanet:33276) |
Lipedema | (Orphanet:77243) |
Malignant peritoneal mesothelioma | (Orphanet:168811) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Menetrier disease | (Orphanet:2494) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Non-histaminic angioedema | (Orphanet:658) |
Osteosclerosis - ichthyosis - premature ovarian failure | (Orphanet:75325) |
PEHO syndrome | (Orphanet:2836) |
PEHO-like syndrome | (Orphanet:99807) |
Polyarteritis nodosa | (Orphanet:767) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
Pulmonary arterial hypertension | (Orphanet:182090) |
Secondary intestinal lymphangiectasia | (Orphanet:90363) |
Senior-Loken syndrome 5 | (OMIM:609254) |
Sialidosis type 2 | (Orphanet:87876) |
Systemic capillary leak syndrome | (Orphanet:188) |
Waldenström macroglobulinemia | (Orphanet:33226) |
Whipple disease | (Orphanet:3452) |