Phenotype #0000045646

Individual ID 00059056
Associated disease HTX1
Phenotype details Heterotaxy, gut malrotation, asplenia, ASD, CAVC, PA
Diagnosis/Initial -
Inheritance Familial, X-linked recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Aimee Paulussen
Database submission license No license selected
Created by Aimee Paulussen
Date created 2016-02-19 12:07:46 +01:00 (CET)
Date last edited N/A

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