Phenotype #0000351744

Individual ID 00466380
Associated disease WRWFFR
Diagnosis/Initial Congenital arthrogryposis
Diagnosis/Definite Wieacker-Wolff syndrome, female-restricted
Phenotype details Arthrogryposis multiplex congenita
Inheritance Isolated (sporadic)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Owner name Camille Verebi
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Camille Verebi
Date created 2025-08-27 08:56:54 +02:00 (CEST)
Date last edited 2026-02-06 10:21:15 +01:00 (CET)

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