Phenotype #0000161991

Individual ID 00213537
Associated disease DA
Phenotype details hypotonia, joint contractures, and bilateral club foot (at birth); ; cannot walk without support
Diagnosis/Initial distal arthrogryposis
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Minttu Marttila
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-08-28 11:29:56 +02:00 (CEST)
Date last edited 2013-08-31 16:16:18 +02:00 (CEST)

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