Phenotype #0000129837

Individual ID 00164822
Associated disease PCH9
Phenotype details Cognitive milestones: Severely delayed
OFC: -3.6 (-4.6 SD)
Cerebellum: Hypoplasia
Pons: Mild hypoplasia
Brainstem: “Figure 8” + Hypoplasia
Corpus callosum: Complete ACC
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite PCH9
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Ashley Marsh
Database submission license No license selected
Created by Ashley Marsh
Date created 2018-06-17 23:31:47 +02:00 (CEST)
Date last edited 2018-06-20 15:04:19 +02:00 (CEST)

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