Phenotype #0000083941

Individual ID 00106135
Associated disease NHS
Phenotype details congenital diaphragmatic hernia (HP:0000776 ), congenital cataract (HP:0000519)
Diagnosis/Initial -
Inheritance Familial, X-linked
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Molka Kammoun
Database submission license No license selected
Created by Molka Kammoun
Date created 2017-06-29 10:41:53 +02:00 (CEST)
Date last edited 2017-06-30 10:04:47 +02:00 (CEST)

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