Phenotype #0000051923

Individual ID 00072218
Associated disease LGMDR3;LGMD2D
Phenotype details proximal muscle weakness (HP:0003701), calf hypertrophy (HP:0008981), loss of ambulation (HP:0002540), no cardiac involvement (-HP:0001627), no respiratory impairment (-HP:0002093)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 03y
Phenotype/Onset Myalgia (HP:0003326)
Protein -
Owner name Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers
Date created 2016-06-01 10:05:32 +02:00 (CEST)
Date last edited 2017-02-18 21:12:09 +01:00 (CET)

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