Cerebral edema

Symptom Information:

Symptom ID: HPO:0002181
Synonyms:
Brain edema [HPO:0002181]
Brain oedema [HPO:0002181]
Brain edema [OMIM:Brain edema]
Cerebral edema [OMIM:Cerebral edema]
Brain oedema [MedDRA:10048962]
Quality:
Cross references:
OMIM: "Brain edema" [OMIM:Brain edema]
OMIM: "Cerebral edema" [OMIM:Cerebral edema]
Is a (Direct Parents):
HPO         Edema
HPO         Abnormality of the cerebrum
MedDRA Cerebral injuries NEC
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)