Phenotype #0000129991

Individual ID 00165096
Associated disease SHFYNG
Phenotype details see paper; ...
Diagnosis/Initial Prader-Willi syndrome-like
Inheritance Isolated (sporadic)
Diagnosis/Definite SHFYNG
Age/Examination 03y06m (3 years, 6 months)
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 14:07:18 +02:00 (CEST)
Date last edited 2025-10-12 16:52:11 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.