Phenotype #0000051292
| Individual ID |
00065184 |
| Associated disease |
ID |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Inheritance |
Isolated (sporadic) |
| Phenotype details |
mild autism (HP:0000729), Microcephaly (HP:0000252), no abnormality of vision (-HP:0000252),; severe intellectual disability (HP:0010864); motor delay (HP:0001270); severe speech delay (HP:0000750) |
| Age/Examination |
05y (5 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Pieter Klap |
| Database submission license |
No license selected |
| Created by |
Pieter Klap |
| Date created |
2016-05-20 15:15:44 +02:00 (CEST) |
| Date last edited |
2020-05-12 12:33:06 +02:00 (CEST) |
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