Phenotype #0000020227

Individual ID 00024129
Associated disease MRT
Phenotype details Severe, non-specific, autosomal recessive intellectual disability
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 05y (5 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Rami Abou Jamra
Database submission license No license selected
Created by Rami Abou Jamra
Date created 2014-10-29 13:07:08 +01:00 (CET)
Date last edited 2014-10-31 15:05:37 +01:00 (CET)

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