Hydrops fetalis
Information
- Disease name
- Hydrops fetalis
- Disease ID
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT03412760 | Enrolling by invitation | N/A | Hydrops: Diagnosing & Redefining Outcomes With Precision Study | October 11, 2018 | December 2025 |
| NCT00143039 | Terminated | Amniotic Fluid Tandem Mass Spectrometry for Pregnancies Complicated by NIH and Severe Symmetrical IUGR | March 2006 | August 2009 |
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0001789
- OrphaNumber from OrphaNet (Orphanet)
- 1041
- MedGen concept unique identifier (MedGen Concept name)
- C0020305
- MedGen unique identifier (MedGen Concept name)
- 6947
- MeSH unique ID (MeSH (Medical Subject Headings))
- D015160