Preeclampsia
Symptom Information:
Symptom ID: | HPO:0100602 | ||||||||||||||||||||||||||||||
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 prenatal development or birth(HPO:0001197) Prenatal maternal abnormality(HPO:0002686) Toxemia of pregnancy(HPO:0100603) Preeclampsia(HPO:0100602) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal hypertension and related conditions(MedDRA:10038466) Preeclampsia(HPO:0100602) |
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Database Frequency: | 9 / 7739 | ||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |
PREECLAMPSIA/ECLAMPSIA 1 | (OMIM:189800) |
PREECLAMPSIA/ECLAMPSIA 4 | (OMIM:609404) |
PREECLAMPSIA/ECLAMPSIA 5 | (OMIM:614595) |
Preeclampsia | (Orphanet:275555) |
THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE | (OMIM:188055) |
Wilson-Turner syndrome | (Orphanet:3459) |