Phenotype #0000155298

Individual ID 00207522
Associated disease MCAHS2;GPIBD4
Phenotype details Global developmental delay; seizures; central hypotonia; brain atrophy
Diagnosis/Initial -
Inheritance Familial, X-linked
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Philippe Campeau
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Philippe Campeau
Date created 2018-11-23 18:14:12 +01:00 (CET)
Date last edited N/A

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