Prenatal maternal abnormality
Symptom Information:
| Symptom ID: | HPO:0002686 | ||||
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of prenatal development or birth(HPO:0001197) Prenatal maternal abnormality(HPO:0002686) MedDRA: |
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| Database Frequency: | 3 / 7739 | ||||
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All diseases associated with this symptom:
| Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
| Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
| Thoracolaryngopelvic dysplasia | (Orphanet:3317) |