Rank (Similarity) |
PMID (PMCID) |
---|
|
Total: 9
HPO ID | Term | Frequency |
---|---|---|
HP:0001541 | Ascites | Very frequent (99-80%) |
HP:0001789 | Hydrops fetalis | Very frequent (99-80%) |
HP:0001873 | Thrombocytopenia | Very frequent (99-80%) |
HP:0001903 | Anemia | Very frequent (99-80%) |
HP:0000478 | Abnormality of the eye | Occasional (29-5%) |
HP:0000504 | Abnormality of vision | Occasional (29-5%) |
HP:0001511 | Intrauterine growth retardation | Occasional (29-5%) |
HP:0001639 | Hypertrophic cardiomyopathy | Occasional (29-5%) |
HP:0010880 | Increased nuchal translucency | Occasional (29-5%) |
Total: 0
HPO ID | Term | # of case reports |
---|
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|