Phenotype #0000344618

Individual ID 00456088
Associated disease CHARGE
Phenotype details HP:0200138, HP:0009603, HP:0000377, HP:0001643, HP:0012020, HP:0002901, HP:0010515
Diagnosis/Initial complex neurodevelopmental disorder
Inheritance Isolated (sporadic)
Diagnosis/Definite CHARGE SYNDROME
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Cleft -
Eye/Orbital -
Protein -
Eye/Ball -
Fistula -
Owner name Marketa Wayhelova
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Marketa Wayhelova
Date created 2024-10-23 09:38:17 +02:00 (CEST)
Date last edited 2024-10-24 10:01:46 +02:00 (CEST)

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