Phenotype #0000129329

Individual ID 00164219
Associated disease MCLMR
Inheritance Familial, autosomal dominant
Phenotype details -
Diagnosis/Initial MCLMR
Age/Examination -
Diagnosis/Definite MCLMR
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Pascal Brouillard
Database submission license No license selected
Created by Pascal Brouillard
Date created 2014-11-25 14:57:17 +01:00 (CET)
Date last edited N/A

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