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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