Phenotype #0000227245
| Individual ID |
00299923 |
| Associated disease |
NLS1 |
| Phenotype details |
HP:0001511, HP:0000340, HP:0000470, HP:0000377, HP:0000369, HP:0000153, HP:0012472, HP:0000218, HP:0000347,HP:0003196, HP:0000463, HP:0007651,HP:0000518, HP:0000252, HP:0001339, HP:0001321, HP:00012714, HP:0000238, HP:0002514, HP:0001371, HP:0001762, HP:0005684, HP:0010557,HP:0008064,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 |
2020-04-21 20:13:55 +02:00 (CEST) |
| Date last edited |
2020-04-22 14:29:00 +02:00 (CEST) |
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