Phenotype #0000238263

Individual ID 00313964
Associated disease ID
Diagnosis/Initial intellectual disability
Diagnosis/Definite WITKOS
Inheritance Familial, autosomal dominant
Phenotype details see paper; ..., intellectual disability (TIQ <70); OFC percentile <P0.6; height percentile P2; MRI brain cortical dysgenesis; autism spectrum disorder; no epilepsy; clinidactyly; no hearing loss; typical facial dysmorphic features; no ectodermal symptoms
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-10-09 15:12:14 +02:00 (CEST)
Date last edited N/A

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