Phenotype #0000025894
| Individual ID |
00032458 |
| Associated disease |
RIEG1 |
| Phenotype details |
no heart defect; no hearing loss; hypospadias; redundant umbilical skin; Axenfeld-Rieger syndrome, glaucoma, vascular loops; hypodontia |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
37y (37 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Elena Semina |
| Database submission license |
No license selected |
| Created by |
Elena Semina |
| Date created |
2012-02-19 20:47:51 +01:00 (CET) |
| Date last edited |
2025-02-03 11:32:17 +01:00 (CET) |
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