Phenotype #0000138573

Individual ID 00173709
Associated disease SMAX-2
Phenotype details -
Diagnosis/Initial X-linked congenital spinal muscular atrophy
Inheritance Familial, X-linked recessive
Diagnosis/Definite SMAX-2
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset ?
Protein -
Owner name Alfons Meindl