Phenotype #0000003011

Individual ID 00004291
Associated disease GCPS
Phenotype details hand bilateral postaxial polydactyly, feet bilateral postaxial polydactyly; no preaxial polydactyly; syndactyly; macrocephaly; widely spaced eyes; corpus callosum hypoplasia, ventricular dilatation; no developmental delay; laryngomalacia
Diagnosis/Initial Greig cephalopolysyndactyly syndrome
Inheritance Familial, autosomal dominant
Diagnosis/Definite GCPS
Age/Examination 04y (4 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Tania Attie-Bitach
Database submission license No license selected
Created by Tania Attie-Bitach
Date created 2014-01-20 11:39:18 +01:00 (CET)
Date last edited 2021-05-24 10:16:24 +02:00 (CEST)

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