Phenotype #0000227019
| Individual ID |
00295970 |
| Associated disease |
NLS2 |
| Phenotype details |
HP:0001511, HP:0000470,HP:0000377,HP:000369, HP:0000347, HP:0000518, HP:0000492, HP:000252, HP:0001339, HP:0001321, HP:00012714, HP:0002514, HP:0001371, HP:0001838, HP:0001762, HP:0008064, HP:0000951, HP:0002089, HP:0003241 |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Fatima Abdelfattah |
| Database submission license |
No license selected |
| Created by |
Fatima Abdelfattah |
| Date created |
2020-04-20 15:11:22 +02:00 (CEST) |
| Date last edited |
2020-04-21 10:01:49 +02:00 (CEST) |
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