Phenotype #0000165272

Individual ID 00216820
Associated disease LGMD
Phenotype details lost ability to walk (HP:0006957) 5y
Diagnosis/Initial limb-girdle muscular dystrophy
Inheritance Isolated (sporadic)
Diagnosis/Definite LGMD1B
Age/Examination -
Age/Diagnosis 12y
Age/Onset <2y
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-03-21 15:55:05 +01:00 (CET)
Date last edited 2020-10-04 11:06:42 +02:00 (CEST)

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