Phenotype #0000143455
Individual ID |
00181269 |
Associated disease |
LIS3 |
Phenotype details |
Agenesis of the corpus callosum (HP:0001274); Agyria-pachygyria (HP:0031883, HP:0001302); Cerebellar vermis hypoplasia (HP:0001320); no Abnormality of brainstem morphology (-HP:0002363); no Gray matter heterotopia (-HP:0002281); Abnormality of the internal capsule (HP:0012502); no Congenital microcephaly (-HP:0011451); Microcephaly (HP:0000252); Infantile spasms (HP:0012469) |
Diagnosis/Initial |
- |
Inheritance |
Isolated (sporadic) |
Diagnosis/Definite |
- |
Age/Examination |
03y00m (3 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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