Phenotype #0000129996

Individual ID 00165095
Associated disease SHFYNG
Phenotype details see paper; ...
Diagnosis/Initial Prader-Willi syndrome-like
Inheritance Isolated (sporadic)
Diagnosis/Definite SHFYNG
Age/Examination 05y (5 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Yutak Negishi
Database submission license No license selected
Created by Yutak Negishi
Date created 2018-06-25 14:52:16 +02:00 (CEST)
Date last edited 2025-10-12 16:50:14 +02:00 (CEST)

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