Phenotype #0000338958

Individual ID 00449812
Associated disease microcephaly
Diagnosis/Initial craniosynostosis
Diagnosis/Definite MCPH27
Phenotype details HP:0000253, HP:0000271, HP:0001363, HP:0001249
Inheritance Isolated (sporadic)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Marketa Wayhelova
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Marketa Wayhelova
Date created 2024-05-16 07:05:59 +02:00 (CEST)
Date last edited 2024-08-20 16:08:24 +02:00 (CEST)

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