Phenotype #0000351948

Individual ID 00466584
Associated disease ?
Diagnosis/Initial multiple congenital abnormalities
Diagnosis/Definite MICPCH
Phenotype details HP:0000253, HP:0004322, HP:0008915, HP:0000518
Inheritance Isolated (sporadic)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Marketa Wayhelova
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Marketa Wayhelova
Date created 2025-09-17 09:40:44 +02:00 (CEST)
Date last edited 2025-09-26 10:52:19 +02:00 (CEST)

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