Eclampsia
Symptom Information:
Symptom ID: | HPO:0100601 | ||||||||||||||||||
Synonyms: |
|
||||||||||||||||||
Quality: | |||||||||||||||||||
Cross references: |
|
||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of prenatal development or birth(HPO:0001197) Prenatal maternal abnormality(HPO:0002686) Toxemia of pregnancy(HPO:0100603) Eclampsia(HPO:0100601) MedDRA: Nervous system disorders(MedDRA:10029205) Seizures(HPO:0001250) Seizures and seizure disorders NEC(MedDRA:10039912) Eclampsia(HPO:0100601) |
||||||||||||||||||
Database Frequency: | 6 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
PREECLAMPSIA/ECLAMPSIA 4 | (OMIM:609404) |
PREECLAMPSIA/ECLAMPSIA 5 | (OMIM:614595) |
Preeclampsia | (Orphanet:275555) |
Wilson-Turner syndrome | (Orphanet:3459) |