Phenotype #0000143968

Individual ID 00183216
Associated disease HCP
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Manuel Mendez
Database submission license No license selected
Created by Manuel Mendez
Date created 2018-10-16 12:40:39 +02:00 (CEST)
Date last edited 2018-10-25 19:43:21 +02:00 (CEST)

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