Phenotype #0000078875

Individual ID 00100647
Associated disease CM1
Phenotype details hypertelorism, prominent head, epicanthus, clinodactyly, psycho-motor delay
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 12y (12 years)
Age/Onset 12y
Phenotype/Onset -
Protein -
Owner name Patrizia De Marco
Database submission license No license selected
Created by Patrizia De Marco
Date created 2017-03-07 16:56:34 +01:00 (CET)
Date last edited 2017-03-09 11:38:07 +01:00 (CET)

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