Phenotype #0000227018
| Individual ID |
00295969 |
| Associated disease |
NLS2 |
| Phenotype details |
HP:0001511,HP:0000340, HP:0000470, HP:0000377, HP:000369, HP:0012472, HP:0000347, HP:000252, HP:0001302, HP:0007364, HP:00012714, HP:0000238, HP:001371, HP:0001838, HP:0009601, HP:0030084 |
| 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 14:48:23 +02:00 (CEST) |
| Date last edited |
2020-04-21 09:57:45 +02:00 (CEST) |
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