Phenotype #0000143477
Individual ID |
00181291 |
Associated disease |
LIS3 |
Phenotype details |
Partial agenesis of the corpus callosum (HP:0001338); Polymicrogyria (HP:0002126); Dysgenesis of the cerebellar vermis (HP:0002195); Microcephaly (HP:0000252) |
Diagnosis/Initial |
- |
Inheritance |
Isolated (sporadic) |
Diagnosis/Definite |
- |
Age/Examination |
04y00m (4 years) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Moritz Hebebrand |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Moritz Hebebrand |
Date created |
2018-10-04 18:03:58 +02:00 (CEST) |
Date last edited |
N/A |
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