Phenotype #0000167954
| Individual ID |
00222752 |
| Associated disease |
IBGC1 |
| Phenotype details |
brain calcifications |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Wanjin Chen |
| Database submission license |
No license selected |
| Created by |
Wanjin Chen |
| Date created |
2019-02-11 11:05:07 +01:00 (CET) |
| Date last edited |
2019-02-11 13:18:02 +01:00 (CET) |
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