Phenotype #0000269368

Individual ID 00374158
Associated disease GCPS
Phenotype details hand bilateral postaxial polydactyly; feet bilateral preaxial polydactyly; syndactyly; macrocephaly; no widely spaced eyes; no developmental delay
Diagnosis/Initial Greig cephalopolysyndactyly syndrome
Inheritance Familial, autosomal dominant
Diagnosis/Definite GCPS
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-05-24 10:55:07 +02:00 (CEST)
Date last edited N/A

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