Phenotype #0000153669

Individual ID 00205498
Associated disease HMN
Phenotype details -
Diagnosis/Initial spinal muscular atrophy
Inheritance Familial, autosomal dominant
Diagnosis/Definite HMN-5A
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 2012-11-05 15:40:28 +01:00 (CET)
Date last edited 2020-04-08 10:52:45 +02:00 (CEST)

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