Phenotype #0000060513

Individual ID 00080944
Associated disease MDDGB6;MDC1C
Phenotype details Muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5 (OMIM:606612)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Daniel Trujillano
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-09-07 13:24:08 +02:00 (CEST)
Date last edited N/A

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