Phenotype #0000257382

Individual ID 00361989
Associated disease RMD2;LGMD1C
Phenotype details Hypotonia HP:0001252
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Ibrahim Sahin
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Ibrahim Sahin
Date created 2021-04-13 11:11:16 +02:00 (CEST)
Date last edited 2021-04-14 15:52:40 +02:00 (CEST)

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