Phenotype #0000086891

Individual ID 00109418
Associated disease UCMD
Phenotype details congenital arthrogryposis, bilateral hip dislocation; severe proximal weakness, distal finger hyperlaxity with long finger contractures; rigid spine; FVC 0.30
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Sandra Donkervoort
Database submission license No license selected
Created by Sandra Donkervoort
Date created 2014-07-10 10:11:45 +02:00 (CEST)
Date last edited 2014-07-11 16:16:24 +02:00 (CEST)

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