Phenotype #0000024946

Individual ID 00027225
Associated disease FMD1
Phenotype details see paper; pansynostosis, broad prominent forehead/brow ridge, micro/retrognathia, camptodactyly/arthrogryposis, no broad/flattened/spatulateterminal digits; long slender digits, flexion deformity elbows, genu valgum, mixed hearing loss
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Stephen Robertson
Database submission license No license selected
Created by Johan den Dunnen
Date created 2015-01-03 10:11:15 +01:00 (CET)
Date last edited 2015-10-11 16:45:55 +02:00 (CEST)

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