Phenotype #0000066680

Individual ID 00087080
Associated disease PRLTS
Phenotype details see paper; profound hearing loss, brain atrophy, lower limb spasticity in early childhood, ...
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
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 2016-11-10 11:41:31 +01:00 (CET)
Date last edited N/A

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