Phenotype #0000143456

Individual ID 00181270
Associated disease LIS3
Phenotype details Agenesis of the corpus callosum (HP:0001274); Polymicrogyria (HP:0002126); no Abnormality of brainstem morphology (-HP:0002363); Cerebellar hypoplasia (HP:0001321); Dilation of lateral ventricles (HP:0006956); no Congenital microcephaly (-HP:0011451); Microcephaly (HP:0000252); no Seizures (-HP:0001250); Optic nerve hypoplasia (HP:0000609)
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 14d
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Moritz Hebebrand
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Moritz Hebebrand
Date created 2018-10-04 18:03:58 +02:00 (CEST)
Date last edited N/A

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