Cerebral edema
Symptom Information:
Symptom ID: | HPO:0002181 | ||||||
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) Cerebral edema(HPO:0002181) MedDRA: Injury, poisoning and procedural complications(MedDRA:10022117) Injuries NEC(MedDRA:10022114) Cerebral injuries NEC(MedDRA:10052638) Cerebral edema(HPO:0002181) |
||||||
Database Frequency: | 19 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Acute necrotizing encephalopathy of childhood | (Orphanet:263524) |
Acyl-CoA dehydrogenase 9 deficiency | (Orphanet:99901) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Argininemia | (Orphanet:90) |
Argininosuccinic aciduria | (Orphanet:23) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Citrullinemia type I | (Orphanet:247525) |
Citrullinemia type II | (Orphanet:247585) |
Classic maple syrup urine disease | (Orphanet:268145) |
Familial acute necrotizing encephalopathy | (Orphanet:88619) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Intermittent maple syrup urine disease | (Orphanet:268173) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
Medium chain acyl-CoA dehydrogenase deficiency | (Orphanet:42) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |
Pyruvate dehydrogenase phosphatase deficiency | (Orphanet:79246) |
Thiamine-responsive maple syrup urine disease | (Orphanet:268184) |