Phenotype #0000157231

Individual ID 00208593
Associated disease CLP
Phenotype details minor anomalies in some affected patients in this family:
hypodontia, dry skin, duplicated thumb
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset congenital
Protein -
Owner name J.H.L.M. (Hans) van Bokhoven
Database submission license No license selected
Created by J.H.L.M. (Hans) van Bokhoven
Date created 2018-12-11 13:35:20 +01:00 (CET)
Date last edited 2018-12-13 15:01:00 +01:00 (CET)

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