| Individual ID |
00417244 |
| Associated disease |
ID |
| Diagnosis/Initial |
intellectual disability |
| Diagnosis/Definite |
- |
| Inheritance |
Isolated (sporadic) |
| Phenotype details |
Global developmental delay (HP:0001263); ; no Seizure (-HP:0001250); no Sensorineural hearing impairment (-HP:0000407); Microcephaly (HP:0000252) ; Ophthalmological anomalies (bilateral iris cysts) |
| Age/Examination |
00y14m (14 months) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Fernanda Soledad Jalil |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Fernanda Soledad Jalil |
| Date created |
2022-09-14 15:36:48 +02:00 (CEST) |
| Date last edited |
2022-11-11 12:45:59 +01:00 (CET) |