Abnormality of the amniotic fluid
Symptom Information:
| Symptom ID: | HPO:0001560 | ||
| Synonyms: |
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of prenatal development or birth(HPO:0001197) Abnormality of the amniotic fluid(HPO:0001560) MedDRA: |
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| Database Frequency: | 7 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| ALG1-CDG | (Orphanet:79327) |
| Hemolytic anemia due to red cell pyruvate kinase deficiency | (Orphanet:766) |
| Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
| Lethal congenital contracture syndrome type 1 | (Orphanet:1486) |
| Milroy disease | (Orphanet:79452) |
| Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
| PMM2-CDG | (Orphanet:79318) |