Phenotype #0000087495
Individual ID |
00111410 |
Associated disease |
ID |
Diagnosis/Initial |
- |
Diagnosis/Definite |
- |
Inheritance |
Isolated (sporadic) |
Phenotype details |
Female, severe ID, behavioral anomalies; severe intellectual disability (HP:0010864); severe global developmental delay (HP:0011344) |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Bernt Popp |
Database submission license |
No license selected |
Created by |
Bernt Popp |
Date created |
2017-08-03 07:39:05 +02:00 (CEST) |
Date last edited |
2020-05-12 12:33:06 +02:00 (CEST) |
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