Phenotype #0000073487

Individual ID 00095093
Associated disease COXPD5
Phenotype details Agenesis of corpus callosum, Hypertrophic cardiomyopathy, Pulmonary hypoplasia, Low-set ears
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Karen Stals
Database submission license No license selected
Created by Karen Stals
Date created 2017-01-06 11:16:57 +01:00 (CET)
Date last edited 2017-01-08 11:43:06 +01:00 (CET)

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