Phenotype #0000227023
| Individual ID |
00295971 |
| Associated disease |
NLS2 |
| Phenotype details |
HP:0001511, HP:0001558, HP:0000340, HP:0000470, HP:0000377, HP:0000369,HP:0012472, HP:0000153, HP:0000218, HP:0000347, HP:0000316, HP:0000518, HP:0000482, HP:000252, HP:0002536, HP:0012639, HP:0001274, HP:0001371, HP:0001838, HP:0012210, HP:0000924, HP:0001627, HP:0008064 |
| 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 15:47:53 +02:00 (CEST) |
| Date last edited |
2020-04-21 10:02:34 +02:00 (CEST) |
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