Phenotype #0000129496

Individual ID 00164364
Associated disease IIAE2
Phenotype details Acute hepatic failure
Hand tremor
Failure to thrive in infancy
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite SCAR-21
Age/Examination -
Age/Diagnosis 00y22m
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Lior Cohen
Database submission license No license selected
Created by Lior Cohen
Date created 2018-05-19 18:27:58 +02:00 (CEST)
Date last edited 2018-06-01 15:24:34 +02:00 (CEST)

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