HELLP syndrome
Symptom Information:
Symptom ID: | MedDRA:10049058 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Abnormality of thrombocytes(HPO:0001872) Thrombocytopenia(HPO:0001873) HELLP syndrome(MedDRA:10049058) |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |