Phenotype #0000027206

Individual ID 00033806
Associated disease FHCL2
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Mariana Kleinecke
Database submission license No license selected
Created by Mariana Kleinecke
Date created 2015-03-05 10:43:58 +01:00 (CET)
Date last edited 2015-03-05 23:23:56 +01:00 (CET)

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