Phenotype #0000078708
| Individual ID |
00100453 |
| Associated disease |
CDCBM7 |
| Phenotype details |
Cerebellar dysplasia;Hypoplasia of the pons;Thin corpus callosum;Abnormality of the basal ganglia;Neurodevelopmental delay;Spastic hemiparesis;Intellectual disability;Congenital microcephaly;Bilateral |
| Diagnosis/Initial |
- |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Enza Maria Valente |
| Database submission license |
No license selected |
| Created by |
Johan den Dunnen |
| Date created |
2017-03-02 12:47:10 +01:00 (CET) |
| Date last edited |
N/A |
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