Occlusive hydrocephalus, congenital
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
| Synonyms: |
|
|
| Quality: | ||
| Cross references: |
|
|
| Is a (Direct Parents): |
|
|
| Is a (Whole tree): |
HPO:
MedDRA: |
|
| Database Frequency: | 2 / 7739 | |
| Resource: |
All diseases associated with this symptom:
| Hypoplasminogenemia | (Orphanet:722) |
| Ligneous conjunctivitis | (Orphanet:97231) |